<<

molecules

Review Dietary Plant : Effects of Food Processing on Their Content and Bioavailability

Leila Arfaoui

Department of Clinical Nutrition, Faculty of Applied Medical Sciences, King Abdulaziz University, P.O. Box 80324, Jeddah 21589, Saudi Arabia; [email protected]; Tel.: +966-0126401000 (ext. 41612)

Abstract: Dietary plant polyphenols are natural bioactive compounds that are increasingly attracting the attention of food scientists and nutritionists because of their nutraceutical properties. In fact, many studies have shown that -rich diets have protective effects against most chronic diseases. However, these health benefits are strongly related to both polyphenol content and bioavailability, which in turn depend on their origin, food matrix, processing, digestion, and cellular . Although most fruits and vegetables are valuable sources of polyphenols, they are not usually con- sumed raw. Instead, they go through some processing steps, either industrially or domestically (e.g., cooling, heating, drying, fermentation, etc.), that affect their content, bioaccessibility, and bioavail- ability. This review summarizes the status of knowledge on the possible (positive or negative) effects of commonly used food-processing techniques on phenolic compound content and bioavailability in fruits and vegetables. These effects depend on the plant type and applied processing parameters (type, duration, media, and intensity). This review attempts to shed light on the importance of more comprehensive dietary guidelines that consider the recommendations of processing parameters to  take full advantage of phenolic compounds toward healthier foods. 

Citation: Arfaoui, L. Dietary Plant Keywords: plant polyphenols; food processing; phenolic content; bioavailability; bioaccessibility Polyphenols: Effects of Food Processing on Their Content and Bioavailability. Molecules 2021, 26, 2959. https://doi.org/10.3390/ 1. Introduction molecules26102959 Recent progress in nutrition and medicine has metamorphosed the way healthcare is conceived and delivered. An international technology-driven revolution is driving this Academic Editors: Jan Oszmianski rapid change from traditional healthcare to precision medicine by establishing unprece- and Sabina Lachowicz dented research programs and networks that prioritize diseases’ prevention and health promotion mainly through lifestyle and diet-based approaches [1]. A recent emerging area Received: 16 April 2021 of precision nutrition focusing on bioavailable and metabolizable proportions of ingested Accepted: 14 May 2021 Published: 16 May 2021 foods with claimed health benefits has been developed. In this context, plant-derived polyphenols have been associated with several health benefits and are considered bioactive

Publisher’s Note: MDPI stays neutral dietary compounds [2]. Polyphenols are the largest group of dietary antioxidants known with regard to jurisdictional claims in for their ability to scavenge free radicals, donate hydrogen atoms, electrons, or chelate published maps and institutional affil- metal cations [3]. Because of these mechanisms, they have protective and preventive effects iations. against several non-communicable diseases (NCDs), including cardiovascular diseases (CVDs), , and [4]. However, the health implications of dietary polyphenols are determined by their bioavailability to a great extent, which is defined as the fraction of polyphenols released from the food matrix, metabolized, absorbed, and able to impose its bioactivity on the Copyright: © 2021 by the author. Licensee MDPI, Basel, Switzerland. target cells or tissues [5]. Several factors influence polyphenol bioavailability, including the This article is an open access article initial content in foods, food matrix, gut microbiota, and food processing [6]. In fact, most distributed under the terms and fruits and vegetables are not usually consumed raw. Instead, they go through industrial conditions of the Creative Commons or domestic processing steps (e.g., cooling, heating, drying, fermentation, etc.) that affect Attribution (CC BY) license (https:// their content, bioaccessibility, and bioavailability. creativecommons.org/licenses/by/ The main purpose of food-processing techniques is to transform raw ingredients into 4.0/). food, or to transform food into other end-products suitable for human or animal consump-

Molecules 2021, 26, 2959. https://doi.org/10.3390/molecules26102959 https://www.mdpi.com/journal/molecules Molecules 2021, 26, 2959 2 of 35

tion. Some specific objectives include extending the shelf life of ingredients and products by inactivating pathogens or contaminating microorganisms, enhancing the bioavailability of otherwise inaccessible , enabling variety in flavor, texture, or aroma of certain foods, and improving the profile [7]. Domestic and industrial processing affect phenolic compounds’ content, antioxidant capacity, bioaccessibility, and bioavailability in different ways. While many food-processing techniques may lead to phenolic compounds’ degradation, some others enhance their absorption and bioavailability [8,9]. The final polyphenol content and bioavailability in processed food depend, therefore, on factors such as the nature of the process, duration of treatment, and food matrix subjected to the processing technique [10]. Since dietary polyphenol consumption has been increasingly proposed as an effective measure in the primary prevention and management of NCDs, it is imperative to consider the effect of food processing on their content and bioavailability. This review aims to summarize the effects of the most common food-processing techniques, either domestic or industrial, on dietary polyphenol content, bioaccessibility, and bioavailability. To introduce the topic, a glance at polyphenol types, sources, health implications, and the concepts of bioavailability and bioaccessibility is provided.

2. Polyphenol Types and Sources The largest antioxidant group present in the human diet is that of phenolic com- pounds, with more than 8000 different structures identified to date [11]. Plants produce these secondary metabolites in response to ultraviolet light or pathogen attacks [12]. The molecular structure is based on one or several aromatic rings and at least one hydroxyl () group. They can either have a simple structure (such as in the case of phenolic acids) or a complex structure (such as in the case of flavonoids). Based on their molecular structure, phenolics are divided into five main groups: phenolic acids, flavonoids, stilbenes, , and [9]. As phenolic acids and flavonoids were mostly investigated in studies reporting the association between food processing and polyphenol content and bioavailability, these two classes are discussed in greater detail.

2.1. Phenolic Acids Phenolic acids are non-flavonoid polyphenols, and their typical representatives are hydroxybenzoic acids (e.g., gallic, p-hydroxybenzoic, vanillic, and syringic acids) and hy- droxycinnamic acids (e.g., ferulic, caffeic, p-coumaric, chlorogenic, and sinapic acids). They exist in bound or free form in fruits and vegetables. Grains and seeds are particularly rich in bound phenolic acids, which are released after acid or alkaline hydrolysis or enzymatic reactions [11]. Good sources of phenolic acids are fruits (apples, cherries, , and their products, such as wine), vegetables (broccoli, lettuce, and tomatoes), legumes, cereals, and coffee beans [13].

2.2. Flavonoids are a large group of polyphenols that typically contain two aromatic rings linked by a heterocycle. Their subclasses are distinguished by structural differences based on this heterocycle [14]. These subgroups include , flavan-3-ols, flavones, flavanones, and flavonols [11]. , flavonols, and flavanones are widely distributed in plants. Flavones and their derivatives flavonols, as well as their acylated products, represent the largest polyphe- nol subgroup [15]. and are, for example, the most commonly found flavonol aglycones, and they alone have approximately 300 different glycosidic combina- tions [15]. The most relevant flavone sources are fruits, , lettuce, and grapes, while flavanones are mostly present in and products based on them [13]. Among all flavanones, and are typical representatives. Good dietary sources Molecules 2021, 26, x FOR PEER REVIEW 3 of 34

Flavones, , and are widely distributed in plants. Flavones and their derivatives flavonols, as well as their acylated products, represent the largest polyphenol subgroup [15]. Quercetin and kaempferol are, for example, the most commonly found flavonol aglycones, and they alone have approximately 300 different glycosidic combinations [15]. The most relevant flavone sources are citrus fruits, parsley, Molecules 2021, 26, 2959 lettuce, and grapes, while flavanones are mostly present in citruses and products 3based of 35 on them [13]. Among all flavanones, hesperidin and naringenin are typical representatives. Good dietary sources of flavonols include plums, apples, , and , with kaempferol and quercetin being the main representatives [13]. of flavonolsFlavanols include are plums,a very apples,complex onions, group and of blueberries, polyphenols, with which kaempferol include and compounds quercetin beingranging the mainfrom representatives monomeric [ 13].-3-ols to polymeric . ProanthocyanidinsFlavanols are a veryare the complex precursors group of polyphenols,, which which include are compoundsproduced under rang- ing from monomeric flavan-3-ols to polymeric proanthocyanidins. Proanthocyanidins are acidic conditions as a result of polymeric chain cleavage [11]. The most commonly the precursors of anthocyanidins, which are produced under acidic conditions as a result identified monomeric flavanols in dietary sources are , epi(gallo)catechin, and of polymeric chain cleavage [11]. The most commonly identified monomeric flavanols their gallates [13]. are mainly present in , grapes, red wine, cocoa, and in dietary sources are catechin, epi(gallo)catechin, and their gallates [13]. Catechins are [13]. mainly present in tea, grapes, red wine, cocoa, and chocolate [13]. AnthocyanidinsAnthocyanidins areare compoundscompounds responsibleresponsible forfor thethe red,red, blue,blue, andand purplepurple pigmentspigments inin fruitsfruits and vegetables, vegetables, flower flower petals, petals, and and some some grain grain varieties, varieties, such such as black as black rice. rice. As they As theyare mainly are mainly present present as , as glycosides, they are they commonly are commonly referred referred to as anthocyanins. to as anthocyanins. Among Amongthe 31 thecurrently 31 currently known known anthocyanidins, anthocyanidins, the themost most frequently frequently identified identified in in plants areare ,cyanidin, ,delphinidin, andand pelargonidinpelargonidin [ 16[16].]. InIn fact,fact, 90%90% ofof thethe structurestructure ofof anthocyaninsanthocyanins isis basedbased onon thesethese compoundscompounds andand theirtheir derivativesderivatives [[16].16]. SeveralSeveral factorsfactors influenceinfluence thethe colorcolor ofof anthocyanins,anthocyanins, suchsuch asas pHpH andand degreedegree ofof hydroxylation.hydroxylation. DependingDepending onon thesethese factors,factors, thesethese phenolicphenolic compounds compounds can can either either give give blue, blue, red, red, or or purple purple colors colors to to plants plants [ 11[11].]. A A widewide rangerange ofof plant-basedplant-based foodsfoods areare goodgood sourcessources ofof thesethese phenolics,phenolics, withwith grapes,grapes, redred wine,wine, berries,berries, andand somesome vegetablesvegetables beingbeing typicaltypical representativesrepresentatives [ 13[13].]. TheseThese diversediverse polyphenol polyphenol sources sources and and types types discussed discussed above above are valuable, are valuable, and there- and foretherefore it is worth it is worth investigating investigating their bioavailability their bioavailability and health and benefits health inbenefits light of in the light scientific of the literaturescientific availableliterature soavailable far. so far.

3.3. Polyphenols’Polyphenols’ HealthHealth BenefitsBenefits Related Related to to Chronic Chronic Diseases Diseases OxidativeOxidative stressstress andand inflammationinflammation areare commoncommon pathwayspathways thatthat drivedrive thethe progressionprogression ofof manymany NCDs.NCDs. AsAs polyphenolspolyphenols impairimpair thesethese processesprocesses [[17],17], incorporatingincorporating higherhigher dosesdoses ofof thesethese compoundscompounds intointo thethe humanhuman dietdiet maymay bebe aa suitablesuitable tooltool forfor primaryprimary prevention,prevention, loweringlowering thethe incidenceincidence andand delayingdelaying thethe onsetonset ofof severalseveral chronicchronic diseases,diseases, includingincluding cardiovascularcardiovascular diseases,diseases, cancer,cancer, obesity, obesity, and and neurological neurological disorders disorders (Figure (Figure1). 1).

Figure 1. Main health benefits of polyphenols related to chronic diseases.

3.1. Polyphenols Consumption and Their Effects on Obesity Animal, , and human studies have shown that dietary anti-inflammatory and antioxidative compounds may increase thermogenesis and energy expenditure, and de- crease inflammation and oxidative stress, thereby facilitating weight loss and/or reducing the rate of metabolic conditions [18]. Some polyphenols with anti-obesity properties are tea catechins, specifically epigallocatechin-gallate (EGCG). In vitro studies on isolated EGCG or extracts have reported their potential to inhibit preadipocyte differentiation, decrease adipocyte proliferation, and induce apoptosis. They also suppress lipogenesis Molecules 2021, 26, 2959 4 of 35

and promote lipolysis and beta-oxidation processes [19]. A preclinical animal study has reported that EGCG and green tea extract facilitate weight loss by lowering adipose mass in mice fed a high-fat diet [20]. Other polyphenols with anti-obesity properties include antho- cyanins, compounds with great antioxidant [21] and anti-inflammatory potential [22]. Few human clinical trials have assessed the obesity-related effects of -rich foods; however, the available data suggest that black and red juice may effectively reduce markers of inflammation and metabolic disease in overweight people [23,24].

3.2. Polyphenols Consumption and Their Effects on Cardiovascular Diseases Oxidative stress has been linked to endothelial dysfunction, which triggers the onset of early atherosclerosis and CVD. Thus, strategies that aim to reduce oxidative stress and in- flammation may be promising to combat CVD-related disorders. In addition, polyphenols can increase NO synthase activity [25], which in turn positively affects flow-mediated di- latation (FMD). Human trial data suggest that oligomeric proanthocyanidins are an efficient dietary intervention for improving plasma lipid profiles and anti-atherogenic components of plasma, as observed in 70 hyperlipidemic subjects [26]. A 6-week supplementation with 162 mg of quercetin per day was reported to improve hypertensive patients’ systolic blood pressure [27]. However, a daily dose of 100 mg quercetin for 12 weeks did not affect blood pressure in 72 healthy overweight and obese subjects, whereas it positively affected endothelial function measured as FMD and circulating endothelial progenitor cell counts [28]. When the findings from randomized controlled trials (RCTs) of polyphenol supplementation were meta-analyzed, it was concluded that polyphenols could exert beneficial effects on LDL-c, HDL-c, FMD, and both systolic and diastolic pressure, thus supporting their implications in primary CVD prevention [29].

3.3. Polyphenols Consumption and Their Effects on Type 2 Diabetes (T2D) Polyphenols and polyphenol-rich products can also ameliorate the risk of T2D. Polyphe- nols are involved in attenuating postprandial glycemic responses, fasting hyperglycemia, and improving insulin secretion and sensitivity. These implications might be explained by their ability to inhibit the digestion of carbohydrates and intestinal glucose absorption, stimulate insulin secretion, modulate the liver-related release of glucose, and trigger both gene expression and cell signaling pathways [30]. Many studies have investigated the efficacy of polyphenol supplementation at the onset of T2D. One meta-analysis of observa- tional studies found that a diet rich in polyphenols (specifically flavonoids) may serve as a tool to prevent the onset of T2D [31]. Regarding specific food groups, tea consumption was reported to be inversely associated with the onset of T2D. A dose–response meta-analysis of cohort studies suggests that consuming 4–6 cups of tea per day may decrease T2D risk by up to 15% [32]. Other polyphenol-rich food groups linked with a reduced risk of T2D include fruits, specifically berries and yellow vegetables [33,34].

3.4. Polyphenols’ Consumption and Their Effects on Cancer Polyphenol supplementation can hamper cancer progression, probably because of their involvement in cancer cell apoptosis. They were also shown to modulate cell cycle signaling and promote cell defense systems [35]. Epidemiological studies have shown that dietary polyphenol intake is linked with lower cancer incidence. For example, one Cana- dian case-control study observed that high dietary flavonoid consumption could reduce lung cancer occurrence [36], while a Korean study confirmed a similar relationship with gastric cancer [37]. Clinical trials also support the notion that polyphenol compounds may exert beneficial effects on disease progression [38,39]. A meta-analysis of 165 prospective and case-control studies did not confirm the association between total flavonoid intake and cancer risk. However, the subgroup analysis confirmed that a higher intake of some flavonoid classes could lower the risk of some , specifically colon, lung, and stomach ulcers [40]. Molecules 2021, 26, 2959 5 of 35

3.5. Polyphenols’ Consumption and Their Effects on Neurological Disorders Finally, the antioxidant properties of polyphenols are important for improving brain health and function. By scavenging free radicals, they facilitate the reduction of brain cell damage [41]. Using animal models with neurocognitive dysfunction, it has been observed that physiological doses of flavonoids may reduce the accumulation of neu- ropathological proteins and improve synaptic plasticity [41]. Observational studies and RCTs suggest that dietary polyphenols, such as those present in berries, grapes, cocoa, and green tea, may modulate processes related to cognitive health [42]. It was also reported that supplementation could enhance both cerebrovascular function and cognition in postmenopausal women, implying that this polyphenol’s presence in the diet may improve cognitive function in this specific population [43]. A meta-analysis study found that polyphenol consumption (that is, those present in , resveratrol, and soy isoflavones) did not significantly affect the scores reflecting global cognitive functions; however, they improved those scores related to verbal learning, memory, and executive functions, while not affecting attention-related scores [29].

4. Bioavailability of Polyphenols Along with the polyphenol content in foods and their distribution in plants, bioavail- ability is an essential factor that directly influences and determines the biological function of polyphenol-rich-food consumption. A distinction between bioaccessibility and bioavail- ability should be made. Bioaccessibility refers to the fraction that mobilizes from the food matrix and reaches the gastrointestinal system, undergoing digestion, absorption into intestinal epithelial cells, and metabolic changes in the intestine and liver [44]. This definition does not include their utilization in target cells or tissues, such as in the case of bioavailability [45]. Bioavailability refers to a fraction released from the food matrix, subjected to digestion, absorption, metabolism in the liver and intestine, and its further distribution to target tissues and cells where it imposes its bioactivity and exerts positive health-related effects. It is complicated to measure bioactivity owing to practical (and ethical) issues; therefore, bioavailability definitions today do not include bioactivity [46].

4.1. Bioavailability and Bioaccessibility Assessment As seen in the previous section, evaluating bioaccessibility is usually carried out by using in vitro methods that simulate digestion, and in some cases, the simulation of uptake by Caco-2 cells is also included [47]. By contrast, bioavailability is measured in vivo as the change in plasma levels (in humans or animals) of that specific compound after an acute or chronic administration of the food matrix containing the investigated compound [48]. According to published literature, analyses of bioavailability and bioaccessibility of polyphenols have been carried out by using both in vitro and in vivo models. The most utilized in vitro method is the static gastrointestinal model, and several modifications have been applied to it, such as the addition of experiments that simulate the oral phase during digestion or colonic fermentation. One of the models that allow the implementation of colon fermentation experiments is the dynamic gastric model, which has been frequently applied to study polyphenol bioavailability. In addition to in vitro models, in vivo assessments have been performed in rats, pigs, and dogs, and the number of clinical trials in humans has been rapidly increasing during the last decade [49].

4.2. Factors Influencing Polyphenols’ Bioavailability It is challenging to conduct bioavailability studies because several different factors influence it (Figure2). Some of them are external, such as environmental factors (rainfall, sun exposure, soil type, etc.) or the degree of ripeness. The composition of the food matrix and the interaction between polyphenols and other dietary components (proteins, fat, carbohydrate, and fiber), as well as the tendency of polyphenols to build complexes with proteins, should be considered when assessing their bioavailability [10]. Molecules 2021, 26, x FOR PEER REVIEW 6 of 34

According to published literature, analyses of bioavailability and bioaccessibility of polyphenols have been carried out by using both in vitro and in vivo models. The most utilized in vitro method is the static gastrointestinal model, and several modifications have been applied to it, such as the addition of experiments that simulate the oral phase during digestion or colonic fermentation. One of the models that allow the implementation of colon fermentation experiments is the dynamic gastric model, which has been frequently applied to study polyphenol bioavailability. In addition to in vitro models, in vivo assessments have been performed in rats, pigs, and dogs, and the number of clinical trials in humans has been rapidly increasing during the last decade [49].

4.2. Factors Influencing Polyphenols’ Bioavailability It is challenging to conduct bioavailability studies because several different factors influence it (Figure 2). Some of them are external, such as environmental factors (rainfall, sun exposure, soil type, etc.) or the degree of ripeness. The composition of the food matrix and the interaction between polyphenols and other dietary components (proteins, fat, Molecules 2021, 26, 2959 6 of 35 carbohydrate, and fiber), as well as the tendency of polyphenols to build complexes with proteins, should be considered when assessing their bioavailability [10].

FigureFigure 2. Main 2. Main factors factors affecting affecting dietary dietary plant polyphenolspolyphenols content content and and bioavailability. bioavailability.

TheThe chemical chemical structure structure of aa specificspecific polyphenol polyphenol determines determines its fateits fate during during digestion digestion in a significant manner. Dietary polyphenols mostly exist as polymers or glycosides, in a significant manner. Dietary polyphenols mostly exist as polymers or glycosides, containing a glycone part (the sugar group) and an aglycone part (the polyphenol). Most containingphenolic compoundsa glycone part resist (the acidic sugar conditions group) an duringd an aglycone gastric digestion part (the [50 polyphenol).], and as they Most phenoliccannot becompounds absorbed in resist their native acidic form conditions (except for during anthocyanins), gastric thedigestion intestinal [50], enzymes and oras they cannotthe colonic be absorbed microbiota in their hydrolyze native them form prior (exc toept absorption. for anthocyanins), Thus, the degree the intestinal of absorption enzymes or ofthe polyphenols colonic microbiota in the intestine hydrolyze greatly depends them prior on the to chemical absorption. structure Thus, and thethe type degree of of absorptionsugar present of polyphenols in the glycosylated in the formintestine [10]. greatly depends on the chemical structure and the typeThe of hostsugar that present ingests in food the containingglycosylated polyphenols form [10]. also influences their metabolism. Specifically,The host therethat ingests are two importantfood containing factors: thepoly intestinalphenols factors also influences and the systemic their metabolism. factors. In fact, the ingested polyphenols undergo several biochemical changes in the small intestine Specifically, there are two important factors: the intestinal factors and the systemic factors. mainly through hydrolyzation to allow their absorption [10]. The non-absorbed In fractionfact, the of polyphenolsingested polyphenols will transit to undergo the colon, whereseveral they biochemical are transformed changes by the in colonic the small intestinemicroflora mainly into otherthrough bioactive glycoside phenolic hydrolyzation metabolites, to followed allow their by structural absorption modifications [10]. The non- absorbedmainly infraction the liver of prior polyphenols entering the will blood transit stream to the [34, 51colon,–53]. Besideswhere they the intestinal are transformed factors, by thethese colonic biochemical microflora transformations into other bioactive of polyphenols phenolic in the metabolites, digestive tract followed and the typeby structural and modificationsproportions ofmainly their derivative in the liver metabolites prior ente dependring the also blood on the stream host systemic [34,51–53]. factors, Besides such the intestinalas gender, factors, age, presence these biochemical of pathologies, transformations and genetics [10 of]. polyphenols in the digestive tract and theFinally, type theand processing proportions techniques of their applied derivative in domestic metabolites or industrial depend settings also influence on the host systemicthe final factors, polyphenol such content as gender, in the age, food pr andesence thus of its pathologies, bioavailability and (Figure genetics2). The [10]. studies investigating these processing-related effects are discussed in the fifth section of this review. Finally, the processing techniques applied in domestic or industrial settings influence4.3. Polyphenols’ the final Metabolism polyphenol Pathway content during in Digestionthe food and thus its bioavailability (Figure 2). Some phenolic compounds are absorbed in the small intestine and those that are not are metabolized in the colon, where glycosides are hydrolyzed into aglycones and further degraded into simple phenolic acids [51,54]. These changes depend on their chemical structure. For example, anthocyanidins are highly unstable and are absorbed as glycoside-

anthocyanins [55]. As they are highly susceptible to gastric conditions, a very low amount of anthocyanins is bioavailable (approximately 0.1% of the intake) [56]. It is generally observed that those phenolics that are absorbed in the colon have lower bioavailability rates than those that undergo these processes in the intestine [50]. The bioavailability of proanthocyanidins is determined by the degree of polymerization. Most of these phenolics pass through the small intestine to the colon, where the colon microbiota modifies them [57]. Those with a lower degree of polymerization undergo more intense modifications, while those with a higher degree form complexes with macromolecules that disables their further modifications and absorption [58]. Diverse phenolic acids and flavan-3-ols are produced by the reactions between proanthocyanidins and the colonic microbiota, and these products Molecules 2021, 26, 2959 7 of 35

undergo further absorption in the colon [58]. In the case of phenolic acids, the small intestine absorbs one part, and the colon absorbs the other [14]. After absorption by epithelial cells, phenolic acids or colonic metabolites reach the liver through the portal vein, and they undergo conjugation processes described as phase II metabolism (methylation, sulfation, and glucuronidation). Some conjugation processes occur in the small intestine; however, the majority occurs in the liver [10]. Almost all plasma phenolics are products of phase II metabolism, and these metabolites determine the biological activity of ingested dietary polyphenols [45]. These extensive metabolic changes produce several metabolites from a single polyphenol. Therefore, the compounds that reach the target cells and tissues where they impose their bioactivity are very different from the original form present in food, chemically, biologically, and in many other ways.

5. Food-Processing Techniques and Their Effects on Polyphenols Content and Bioavailability Vegetables and fruits are a main source of phenolic compounds. For example, several fruits as apple, berries are very rich in polyphenols with more than 200 mg per 100 g of fresh fruits [59]. However, the content and the bioavailability of these phenolic compounds are influenced by the food-processing technique(s) applied. For instance, and since many food- processing methods involve heat treatment, it is believed that higher temperatures may lead to detrimental changes in fruits and vegetables in terms of their nutritional profile; however, some studies observed quite the opposite [8]. A detailed analysis of 161 polyphenols and their food-processing changes reported that domestic cooking induced notable losses in polyphenols, with great variability between the foods. It was also observed that the food that was investigated was often a more important factor than the process employed, thus highlighting the importance of the food matrix [60]. Many other factors influence the fate of polyphenolic compounds during food processing, and these relationships are briefly presented in the following subsections, depending on the type of food-processing technique used at both industrial and domestic sittings (AppendixA Tables A1 and A2).

5.1. Thermal Processing 5.1.1. Heat Treatment Heat treatments are commonly applied in food processing in both domestic and industrial settings. These treatments include boiling, frying, steaming, baking, stewing, and roasting in traditional, microwave, and steam ovens. Heat is also utilized in other traditional transformation processes such as toasting, coffee roasting, drying, canning, pasteurization, and sterilization. The fate of polyphenols during thermal processing largely depends on the method applied. The heat ruptures cell walls, enabling the bound phenolics to mobilize to other parts of the plant, enhancing their availability [61]. However, at the same time, they are more prone to oxidation, and some are more or less thermostable. Studies applying thermal treatments have shown that boiling causes the most detri- mental polyphenol composition changes in treated samples. Steaming and frying can preserve higher amounts of these compounds. The underlying reason might be that phe- nolics are water-soluble, and during the boiling process, they leak into the surrounding medium (water). As heat treatment decomposes the tissue, it enables the migration of cellular components and nutrients into the boiling water [62]. It has been proposed that polar media (water) might be responsible for higher losses due to polyphenol solubil- ity in water, while nonpolar media (oil) would extract lower amounts of lipid-insoluble polyphenols [63]. The detrimental effects of boiling were observed in the case of onions and asparagus. A 60 min boiling process led to a 20.6% and 43.9% loss in overall flavonol content in onions and asparagus, respectively. Notable changes were also observed in the antioxidant capacities [64]. This was confirmed in another study, in which boiling for 1 h induced 53% and 44% degradation of quercetin diglucoside and monoglucoside in onion bulbs, Molecules 2021, 26, 2959 8 of 35

respectively, while boiling for 30 min, frying, and roasting (in microwave and oven) caused less severe changes [65]. The higher degradation of quercetin derivatives might have occurred because of the difference in the surrounding medium, where water as a polar medium led to a higher extraction of these compounds than oil and air. However, this study also points to the polyphenol class being an important determinant—in the case of anthocyanins (cyanidin 3-, cyanidin 3-laminaribioside, and cyanidin 3-(600- malonylglucoside) and cyanidin 3-(600-malonyl-laminaribioside), frying caused the most severe effects, followed by boiling and roasting [65]. Water volume can also influence the degree of polyphenol alteration during heat treatment. Cooking in smaller volumes resulted in higher phenolic content in zucchini (specifically ), beans (rutin and ), and carrots (). Accordingly, cooking in smaller water volumes yielded lower phenolic concentrations in the surrounding water than cooking in larger volumes [66]. Musilova et al. explored variety as an influencing factor that modulates the relation- ship between food processing and polyphenol alterations. Four sweet potato varieties were subjected to four different heat treatments (boiling, steaming, microwaving, and baking). In general, heating had adverse effects on levels. Boiling was shown to have the most detrimental effect: it lowered the levels of chlorogenic acid by 29% (in the 414-purple variety from Slovakia), neochlorogenic acid by 69% (in the 414-purple variety from Croatia), and trans- by 29% (in the Beauregard variety from Croatia). In contrast, all these treatments increased the levels of total polyphenols, total anthocyanins, and total antioxidant activity, mostly in all analyzed samples [67]. Different boiling periods yielded different polyphenol profiles in foods. For example, blanching (short-interval boiling) of kale leaves led to a 51% decrease in polyphenol content (phenolic acids, flavones, flavonols, and anthocyanins), the lowest of which was observed in the case of (28%) and the highest in ferulic acid (55%). However, cooking for a longer time caused more severe damage, resulting in a 73% decrease in the total polyphenol content [68]. Chumyam et al. highlighted the role of the medium in their study by comparing the utilization of water as a medium (in the case of boiling and steaming) and no medium (in the case of microwaving). All procedures were conducted in 5, 10, and 15 min. All treatments significantly increased antioxidant capacity and total phenolic content in purple skin eggplant compared with raw samples. Boiling yielded samples with the lowest levels of total polyphenols [69]. Of all the methods investigated, 10-min microwaving resulted in the highest total phenolic level and highest antioxidant capacity. In addition, 10-min microwaving proved to be the best method for enhancing the antioxidant capacity of eggplant fruits [69]. The authors proposed that phenolic and antioxidant compounds activated by microwaving remained in eggplant fruits, while cooking by boiling and steaming caused their leakage (either directly or indirectly) into water. High-temperature regimes are also applied to preserve food by inactivating enzymes and pathogen microbes, with sterilization and pasteurization as two commonly applied treatments. In white beans, sterilization significantly decreased the total polyphenol content after 4 and 12 months of storage (by 30 and 46%, respectively). However, these findings may be biased by the effects of storage. This was also observed in condensed tannins; after 12 months of storage, the concentration of these compounds was lower by 30% [70]. Pasteurization of apple juice by conventional high-temperature/short-time treatment also led to notable losses in total polyphenols (by 32.3%). However, pasteurization with pulsed electric field treatment reduced their levels by only 14.9% [71]. Studies have also assessed the effects of thermal processing treatments on the bioavail- ability of dietary polyphenols. Domestic cooking of cherry tomatoes increased the bioavail- ability of naringenin and chlorogenic acid in five test subjects [72]. Mechanical and heat treatments applied during tomato sauce production also enhanced the plasma concentra- tion and urinary excretion of naringenin glucuronide. This was observed in a randomized controlled trial in which eight healthy volunteers ingested either tomato sauce or raw toma- Molecules 2021, 26, 2959 9 of 35

toes [73]. These data confirm that heat treatment enhances the mobilization of polyphenol bioactive compounds from the food matrix, making them more bioavailable. The type of heat treatment is an important determinant of polyphenol bioavailability. When cassava samples were subjected to different cooking methods, the highest total phenolic content was observed in steaming, followed by microwaving and boiling. These cooking methods similarly affected their availability in the subjects, although with only slight differences, steamed samples showed a 74.5% bioavailability, while boiled and microwaved samples obtained similar values (72.9% for boiled and 72.7% for microwaved samples) [74]. Streaming was the best heat method, probably due to the indirect exposure to the polar medium (water); thus, the polyphenols were retained to a higher degree in the plant. The form in which phenolics are present is a well-recognized factor, as observed in carrots when exposed to heating in a microwave oven for 12 min. Although it did not affect anthocyanin bioavailability, it increased the relative urinary recovery of non-acylated anthocyanins without affecting the acylated anthocyanins. The authors proposed that the acylation of anthocyanin derivatives is an important factor when investigating their bioavailability [75]. Finally, Rodriguez-Mateos et al. [76] investigated how baking affected the content and bioavailability of polyphenols, namely anthocyanins, , and phenolic acids. This RCT involving 10 healthy subjects used a baked product containing blueber- ries, an unprocessed blueberry drink, and a matching control baked product. Processing induced no significant changes in the total polyphenolic content; however, it significantly lowered the amounts of anthocyanins (−42%), increased the levels of chlorogenic acid (23%), and significantly enhanced the concentrations of flavanol dimers and trimers (36 and 28%, respectively). By determining the plasma levels of 22 metabolites assessed individ- ually after ingestion of the test products, the authors observed that the blueberry baked product induced mainly an increase in four metabolites (m-hydroxyphenylacetic, ferulic, isoferulic, and hydroxyhippuric acids) and a decrease infour others (hippuric, benzoic, salicylic, and sinapic acids) compared with the blueberry drink, without affecting the bioavailability of the total phenolic levels [76].

5.1.2. Canning Canning is a process that aims to produce commercially sterilized and microbiologi- cally safe products by applying heat treatment. Canned food products can be produced by using retorts, pasteurizers, or heat exchangers. The main aim of heat treatment is to eliminate pathogens or microorganisms that can cause contamination, while metal contain- ers, glass jars, and retort pouches are used to prevent spoilage by new microorganisms. After heating, the canned product is cooled and stored at room temperature to maintain the stability and integrity of both the food and the container/jar used [77]. Canning is reported to reduce total phenolic and flavonoid contents, mostly because phenolic compounds leach into the surrounding medium (brine or syrup) [78]. This extensive leaching results from the applied heat treatment, which disintegrates the cells and tissues, enabling the migration of polyphenols into the medium. There is also a difference in how the canning process is carried out and the correspond- ing conditions. One study examined the differences in the effects of domestic and industrial canning on apricots. Thermal processing imitating industrial conditions induced a higher loss of total phenolics (13–47%), while domestic processing led to lower losses (2–33%). This is proposed to be the consequence of the difference in temperature regimes, the more intensive one being employed in industrial processing. Procyanidins were similarly af- fected: the loss in domestic treatments was 2.4%, and that in industrial treatments was 44%. Phenolic acids (hydroxycinnamic acids, 3-O-caffeoylquinic acid, and 5-O-caffeoylquinic acid) exhibited a significant decline in both thermal processes; however, the greater loss was observed in industrial canning [79]. Molecules 2021, 26, 2959 10 of 35

Interestingly, it has also been reported that canning may lead to the production of some desirable compounds that are not naturally present in raw foods. Investigation of canned showed that the retorting process damaged some phenolic compounds (resveratrol, caffeic acid, and catechin); however, (a belonging to the class of soy isoflavones), which was not measured in raw, was quantified in the canned [80].

5.1.3. Drying Drying is a preservation process that aims to reduce the moisture content of food by using heat and mass transfer [81]. As fruits and vegetables are prone to microbial and biochemical spoilage due to their high water content (which can be more than 80%), drying reduces the water activity and makes a stable end-product with an extended shelf life. Some of these methods include vacuum-drying, solar-drying, air-drying, and freeze-drying. Since drying involves heat treatment, the temperature regime affects the degree of degradation of dietary polyphenols, as observed in jujube fruits. Jujube fruits were sub- jected to different drying procedures: vacuum–microwave (480, 120 W), hot air (70, 60, and 50 ◦C), and combined methods such as pre-drying and finish-drying (60 ◦C + 480/120 W). Freeze-drying (the control treatment) was the most efficient method for preserving total phenolic content, while hot-air-drying caused the greatest loss in these compounds; the highest losses were observed after applying the highest temperature. The polyphenol content was less affected when the methods were combined. Similarly, antioxidant activity was the highest in freeze-dried samples; high air temperature (60 or 70 ◦C) caused detri- mental changes to antioxidant compounds [82]. In cocoa beans, total polyphenol content decreased with an increase in temperature, with the highest decrease being observed at 60 ◦C, and the lowest at 40 ◦C. These detrimental processes may be the result of oxidation and cellular destruction. Moisture content in beans can also be another limiting factor, as it affects the volatility of these compounds and the degree of polyphenol solution [83]. However, the variability of the effects caused by drying is also influenced by the variety and polyphenol class. One study assessed how two drying treatments—one involving air-drying at 55 ◦C and the other at 75 ◦C—affected two apricot cultivars. Interestingly, chlorogenic and neochlorogenic acid contents were observed to increase in the higher temperature regime (in one cultivar), and catechin levels showed the same trend in both cultivars. The authors proposed that polyphenol oxidase remained active to a great extent and that its activity affected the higher production of these two phenolic acids. However, the flavonol content decreased proportionally with the increase in temperature, as well as the content of epicatechin [84]. In some cases, the lowest temperature was not the best solution for retaining high polyphenol levels in the samples but optimizing the temperature and drying period. In a study on cocoa beans at three temperature regimes (drying at 60, 70, and 80 ◦C), the maximum concentration of total phenolics was reported to be in samples that were dried at 70 ◦C, and their levels decreased as the heating procedure was prolonged [85]. In another study, the researchers subjected several fruits (raspberry, boysenberry, redcurrants, and blackcurrant fruit) to drying at 50 ◦C for 48 h, 65 ◦C for 20 h, or 130 ◦C for 2 h until a moisture content below 15% was reached. Drying at 65 ◦C was the best method in terms of the total polyphenol content and radical scavenging activity. Higher temperatures and longer regimes proved to be detrimental to the polyphenols in berries. Specifically, anthocyanin levels were similar in berries dried at 50 and 65 ◦C. However, temperatures above 100 ◦C caused the most detrimental effects on all the analyzed parameters [86]. According to the available literature, drying procedures may be used to obtain prod- ucts with more bioavailable polyphenols. However, the final effect depends on the specific polyphenol class or the individual compounds investigated and the temperature regime. Kamiloglu et al. investigated the effect of home processing on the availability of total phenolics and flavonoids in tomatoes by employing an in vitro gastrointestinal digestion model. They observed that oven drying (70 ◦C for 36 h) yielded a two-fold higher bioavail- Molecules 2021, 26, 2959 11 of 35

ability of total polyphenols; however, this was not the case with total flavonoids [87]. In another study, Kamilo˘gluand Capanoglu (2013) observed that an 8 d sun-drying proce- dure at 30 ◦C positively affected the bioaccessibility of chlorogenic acid, while adversely affecting rutin and anthocyanins (cyanidin-3-glucoside (C3G) and cyanidin-3-rutinoside) in yellow and purple figs, which were undetectable after in vitro digestion [88]. Finally, when conventional hot-air-drying in an oven (60 ◦C for 24 h) was compared with freeze-drying, the authors observed that oven-drying induced more favorable changes in pumpkin flour. The oven-dried samples had higher phenolics, bioaccessible phenolics and phenolic acids, and antioxidant activities [89].

5.2. Cold Processing Freezing is a preservation technique that leads to the formation of water crystals and ice below the freezing temperature, thus slowing down biochemical and physicochemical reactions. Consequently, it stops the activity of most pathogenic microorganisms and enables longer shelf life of foods [90]. Chilling or cooling also reduces microbial and biochemical alterations in foods to maintain stability but to a lesser degree (the temperature range is between −1 and 8 ◦C). Cooling decreases the initial temperature of the food product and maintains its quality for a longer period [90]. The literature mainly points to these low-temperature regimes as non-invasive meth- ods for preserving polyphenols in foods, as observed by Korus and Lisiewska, who con- cluded that freezing of either blanched or cooked kale leaves did not induce notable changes while freezing decreased the polyphenol levels by 3% and their antioxidative activity by 7% [68]. In addition, freezing at −30 ◦C of fresh red raspberries did not alter their antioxi- dant capacity or phenolic levels, measured as total phenolics, anthocyanins, lambertianin C, sanguiin H-6, and [91]. However, in some cases, these techniques can even enhance the content of polyphenols, such as in maqui fruits in which cooling (5 ◦C) and freezing (−20 ◦C) increased the total polyphenol concentration. The frozen samples had higher levels of anthocyanins, and the changes were variable. In addition, the freezing technique was better in terms of preserving these antioxidants, as they were present in these samples even after six months of storage [92]. One of the most important factors that affect the degree of dietary polyphenol preser- vation during food freezing is the freezing rate, as observed in a study that reported that slow-frozen had lower levels of monomeric anthocyanins than quick-frozen ones [93]. Similarly, Poiana et al. observed that individual quick freezing had no significant effect on polyphenolic compounds (total phenolic content, total monomeric anthocyanins) in three berries: blueberry, red raspberry, and [94]. The proposed mechanism is based on the nature of crystal formation. Freezing is a process that leads to the formation of ice crystals, making solutes (such as anthocyanins) localized and relocating the water molecules in the cell structure. Quick freezing induces the formation of smaller crystals, and consequently, the cells undergo less damage during the freezing process. The thawing process will also lead to a lower phenolic loss in quick-frozen samples because less water migrates in the quickly frozen strawberries, and consequently, less polyphenols as well [93]. Literature on the effects of freezing/cooling on dietary polyphenol bioavailability is scarce. One study reported that freezing by immersion in liquid nitrogen and freeze-drying at −50 ◦C decreased the levels of total polyphenols and antioxidant activity in apples, both before and during in vitro gastric digestion. Raw apples, which served as control samples, retained the highest amount of polyphenols and exhibited small decreases in total polyphenol concentrations and antioxidant activity during in vitro gastric digestion [95]. As mentioned above, freezing can damage the food matrix due to ice crystal formation, especially in slow freezing. Consequently, polyphenols have been proposed to undergo higher extraction during digestion, which would enhance their bioavailability. At the same time, they are also more prone to oxidation and degradation, especially when food undergoes thermal treatment after freezing. Accordingly, it could be expected that freezing Molecules 2021, 26, 2959 12 of 35

would have significant effects on polyphenol bioavailability; however, there are no data to address this question [45].

5.3. Biochemical Processing Fermentation Fermentation is a non-thermal process based on the activity of specific microorganisms and their enzymes that induce chemical alterations in food components, leading to a significantly transformed food product. Examples of such food products are fermented milk products (yogurt or cheese), bread, vegetal probiotic beverages, and alcoholic beverages. Today, these processes are well controlled and can yield products with desired characteristics by selecting an appropriate bacteria or yeast [96]. Fermentation is an affordable technique that transforms grains into edible foods by increasing their nutrient bioaccessibility and by positively affecting their antioxidant profile and activity in the end-products. Adebo et al. found higher levels of catechin, , and quercetin in samples of fermented whole grain , while the total flavonoid content, total content, and total phenolic content decreased [97]. The authors proposed that these decreases can be explained by the degradation and hydrolysis of the phenolic compounds, while the increase might be the consequence of fermentation by Lactobacillus strains. Another study reported an increase in total phenolic content in whole grain millet-koji, which might result from the mobilization of phenolic compounds from their bound form into a free form by the activity of the fermentation-produced enzymes [98]. Legumes have also been investigated as food classes in several studies. Eight com- monly consumed legume varieties (black cow gram, mottled cowpea, speckled kidney beans, lentils, small rice beans, small runner beans, and two soya beans) were subjected to fermentation by naturally present bacteria and lactic acid bacteria. All fermented legumes had a high total phenolic content, probably owing to the biotransformation between bound and soluble phenolics. Thus, fermentation in legumes increases the bioavailability of polyphenols [99]. In four underutilized legumes (pigeon pea, Bambara groundnut, African yam bean, and kidney bean), a 4-day fermentation period increased the free soluble phenol content, whereas the bound phenolics were decreased. Free soluble phenolic compounds from fermented samples had a significantly higher reducing power, free radical scavenging ability, and inhibition of lipid peroxidation than the unfermented samples, confirming that fermentation led to enhanced antioxidant activity in the legumes [100]. Thus, in both cases, fermentation led to products with better nutrient profiles and antioxidant characteristics. As observed in the case of heat treatment, the variety determines how fermentation affects polyphenol compounds as well. Fermentation of five different varieties of apple juice led to variable changes in the phenolic profile. In the three varieties, the levels of total phenolics remained the same after the process; however, in two of them, they decreased [101]. However, studies assessing the role of fermentation in improving red grape polyphe- nol bioavailability have indicated that fermentation may play a minor role. In a trial involving nine volunteers ingesting equal amounts of red wine and red grape juice (result- ing in almost equal concentrations of anthocyanins), the authors observed higher urinary excretion of total anthocyanins in the case of juice (0.23%) than in wine (0.18%). They also reported that urinary recovery of five individual anthocyanins was different between the two grape products, without reaching significance in both. Thus, they suggested that these results might be because of the presence of ethanol in red wine [102]. This was not confirmed by Bub et al. [103], who compared the absorption of -3-glucoside between red grape juice, red wine, and dealcoholized red wine. The bioavailability of this compound was similar when volunteers consumed regular wine or those without ; however, it was two-fold higher in the case of juice consumption. According to these results, it cannot be concluded that the ethanol produced by fermentation affects the accessibility of these red grape polyphenols. Molecules 2021, 26, 2959 13 of 35

Black tea is another fermented polyphenol-rich beverage widely consumed in the human diet. Both green and black are a great source of monomeric flavanols (catechins). The difference between these two types of tea is in the production process. Green tea is a product obtained by drying leaves of Camellia sinensis, while the production of involves an additional fermentation step, resulting in the synthesis of oligomeric polyphenolic compounds from catechins. Thus, black tea contains lower levels of these flavanols than green tea [104]. In a trial comparing the absorption rate of catechin derived from black and green teas, the authors concluded that the tea variety did not determine the bioavailability of these flavonols. Plasma kaempferol and quercetin levels were similar in both cases, implying that fermentation did not affect the availability of polyphenols from the matrix [105].

5.4. Mechanical Processing 5.4.1. Peeling Peeling is one of the necessary preparation steps for both industrial and domestic food processing. Peels of many fruits and vegetables contain higher concentrations of bioactive compounds than the rest of the fruit. Some of them are discarded as agro-waste and can be utilized as such for extracting these valuable compounds. For example, citrus peels are abundant in phenolic compounds, such as flavanones, flavones, flavonols, and anthocyanins [106]. Peels of some common fruits (apple, , mandarin, and nectarine) are sources of non-extractable polyphenols [107]. The effects of peeling on polyphenol content have been scarcely addressed in literature. In some cases, this preparation step does not considerably affect the food item’s antioxidant capacity, as it is consumed without the peel, as in the case of and citruses. However, it should be noted that, for example, the white layer in citruses is abundant in polyphenols; thus, a higher degree of peeling and removal of this layer would also lead to a lower polyphenol content in the consumed fruit. In addition, some fruits and vegetables can be consumed either with or without peels; thus, the difference in the polyphenol levels can be significant. Studies have mainly focused on determining the phenolic composition and antioxidant activity of peels. However, few studies have addressed the effect of peeling on dietary polyphenols. For example, a study investigating how different heat-treatment regimes influenced onion flavonoids (quercetin and kaempferol) showed that the preprocessing step (peeling and trimming) caused the greatest loss in flavonoid content in onions (up to 39%) [108]. As onions contain multiple layers, the authors peeled only one layer in some cases and peeled several layers in other cases, resulting in a significant decrease in flavonoid content. This decrease in the flavonoid content could be because 90% of quercetin can be found in the first and second layers in onions [109]. Peeling of fruits and vegetables prior to processing was also observed to diminish phenolic bioactives. For example, peach puree containing peel tissues that underwent blanching and pasteurization had 7–11% higher antioxidant activity (measured by the β-/linoleic acid assay) compared with the puree without the peel [110]. In an- other study, peeling caused a 13–48% loss in total phenolics in peaches, ranging between 316 and 397 mg kg−1 in peeled samples and between 376 and 609 mg kg−1 in unpeeled samples [111]. In the case of wine fermentation, there is also a big difference in whether the process is obtained with or without grape skin. Two white wine varieties were subjected to maceration at 5 ◦C for 24 h and further fermented with Saccharomyces bayanus BC commercial yeast. The authors reported that the total polyphenol index (representing the level of total polyphenols) and total flavonoids increased with an increase in alcohol content and the degree of fermentation. Higher increases were observed in the samples that contained skins, probably owing to a higher degree of polyphenol extraction [112]. Molecules 2021, 26, 2959 14 of 35

5.4.2. Grinding Grinding is a processing technique to reduce the size of solid particles, using mechan- ical forces [113]. It has been applied in the preparation of fruit and vegetable powders, , tea, and coffee, as well as flour production. Most studies that assessed how grinding affected polyphenol content in the raw food material showed that the extraction of these antioxidants was mostly enhanced. However, this largely depends on the particle size of the powder end-product. Grinding of Hieracium pilosella L. (an invasive weed famous for its antiseptic, an- tibacterial, and anti-inflammatory properties) yielded powders with enhanced antioxidant capacity, which was followed by an increase in the content of identified flavonoids and phenolic acids. However, this was observed only in the case of two fractions, which implies that the granulometric class needs to be optimal to obtain the highest degree of extraction of bioactive compounds and their corresponding activity [114]. Another study explored the difference in phenolic content between three types of coffee: Turkish, Espresso, and American coffee. In the case of American and Espresso coffee, fine–coarse powder exhibited the highest total polyphenol content and corresponding antioxidant activity, while in the case of Turkish coffee, fine–coarse and coarse powders were similar. When comparing these three coffees, which differ according to the brewing method, Espresso exhibited the highest antioxidant content and capacity, followed by Turkish and American coffee [115]. In tea, the reduction in the particle size of green tea leaves led to a higher decrease in almost all catechins measured [116]. However, in some cases, the granulometric characteristics do not influence the degree of bioactive extraction caused by grinding. For example, superfine grinding of green propolis enhanced the extraction of bioactive compounds, resulting in increased total phenolic content and antioxidant activity, regardless of the particle size [117]. An overview of studies investigating the effects of the main food-processing tech- niques (type, procedure, food matrix, and investigated polyphenol), and their effects on polyphenols content and bioavailability/bioaccessibility were presented in AppendixA (Tables A1 and A2) respectively.

5.5. Emerging Food-Processing Technologies Other emerging food-processing technologies, such as pulsed electric field, ultrasound treatments, high-pressure, and pulsed-light processing, have been developed in order to enhance the nutritive value, sensory properties, safety and preservation of several food components, including the improvement of polyphenol bioavailability in fruits and veg- etables [45,118]. Through several physical and biochemicals changes of food components, these technologies contribute in reducing some food-related factors that impede polyphe- nols digestion, improving therefore their bioaccessibility and bioavailability [119]. The magnitude of these changes of the physicochemical and functional properties of food bioac- tive ingredients depends on the processing technology, the process parameters/conditions, and the food matrix [119,120]. Since we focused primarily on conventional food processing used at both domestic and industrial settings, these emerging technologies are beyond the scope of this review. However, it is important to investigate further their potential beneficial effects on dietary phytophenols in future studies and reviews to optimize their process- ing conditions according to each food matrix in order to maximize their bioaccessibility, bioavailability and health benefits.

6. Conclusions As a large body of research evidence strongly supports the use of polyphenol-rich foods in the primary prevention and management of various chronic diseases, estimating their bioavailability is of great importance to draw straightforward conclusions regarding their actual efficacy. Since many fruits and vegetables are required to undergo food prepa- ration prior to consumption, the summarized data regarding its influence on polyphenol content and bioavailability provide valuable insights into the actual benefits that could Molecules 2021, 26, 2959 15 of 35

be obtained after consumption. Among the reviewed treatments that apply thermal pro- cessing, boiling is frequently reported to cause the most severe degradation in polyphenol content and bioavailability, mainly owing to their extensive leaching from the food matrix into the surrounding polar medium. Other treatments that utilize heat (such as canning and drying) have reported variable results. In canning, the presence of the surrounding medium plays an important role, while the intensity of the temperature regime and the du- ration of the process influence the end polyphenol content both when canning and drying are applied. Fermentation is reported to mainly lead to desirable changes in polyphenol content in food; however, bioavailability studies do not support the importance of fermen- tation in wine and black tea. Pickling can also yield products with an improved polyphenol profile, and studies have highlighted that this effect was mostly observed after an adequate fermentation period. Freezing and chilling are preservation techniques that are generally considered to produce minimal alterations in dietary polyphenols. Grinding is applied to facilitate the extraction of bioactive compounds, and this was mainly observed in polyphe- nols, with the particle size influencing their content. Data on the polyphenol-related effects of peeling are scarce; however, the existing evidence suggests that removing external layers can reduce the levels of polyphenols (and supposedly their bioavailability) in fruits and vegetables that contain polyphenol-rich peels (such as in the case of citruses). Although the bioavailability of polyphenols has gained popularity in the research community during the last decade, few studies have addressed this issue with regard to their bioavailability as influenced by food processing.

Funding: This research received no external funding. Institutional Review Board Statement: Not applicable. Informed Consent Statement: Not applicable. Data Availability Statement: Data sharing not applicable. Conflicts of Interest: The author declares no conflict of interest. Molecules 2021, 26, 2959 16 of 35

Appendix A

Table A1. Overview of studies investigating the food-processing effects on polyphenols content and antioxidant activity.

Effects on Polyphenols Content and/or Food Processing Procedure Food Matrix Investigated Polyphenols Reference Antioxidant Activity Thermal Processing Flavonols decreased by 20.6% in onions and by 43.9% Boiling for 60 min Onions and asparagus Flavonols in asparagus [64] Antioxidant activity decreased by 10.65%. Cooking in small water volumes caused a decrease by 11.1% in rutin (zucchini), by 1.8% in rutin (beans), by Rutin (zucchini), rutin and 0.9% in quercetin (beans), by 25.4% in chlorogenic acid Cooking in smaller and larger Zucchini, beans, quercitrin (beans), chlorogenic (carrots), and by 38.6% in caffeic acid (potatoes). [66] amounts of water carrots, potatoes acid (carrots), caffeic acid Cooking in larger water volumes caused a decrease by (potatoes) 30.6% in rutin (zucchini), by 29.7% in rutin (beans), by 26.7% in quercetin (beans), by 62.8% in chlorogenic acid (carrots) and by 42.3% in caffeic acid (potatoes). NS difference in meals containing raw and cooked Cooking 15 min at 100 ◦C Cherry tomato Naringenin and chlorogenic acid tomatoes, however, the content of analyzed [72] polyphenols was higher in those with raw tomatoes. Microwave (900 W) cooking Acylated and non-acylated Decrease in both acylated (by 22.93%) and non-acylated Purple carrots [75] Heat treatment for 12 or 20 min anthocyanin content (by 22.52%) anthocyanin content. Pasteurization (HTST—90 ◦C for 30 s and PEF 4 µs bipolar pulse with an electric field TPC after HTST pasteurization decreased by 32.3%. Apple juice TPC [71] strength of 35 kV/cm and a TPC after PEF pasteurization decreased by 14.49%. frequency of 1200 pulses per second) Oven-roasting Quercetin diglucoside decreased after all treatments. (180 ◦C/15 min and Quercetin monoglucoside decreased after microwaving 200 ◦C/30 min); frying and boiling and increased after frying and (180 ◦C/4 min and oven-roasting. Onions Flavonols and anthocyanins [65] 180 ◦C/8 min); microwaving All anthocyanins (cyanidin 3-glucoside, cyanidin (450 W/4 min and 3-laminaribioside, cyanidin 3-(600-malonylglucoside), 750 W/4 min); boiling (for 30 cyanidin 3-(600-malonyl-laminaribioside) decreased and 60 min) after all treatments. Molecules 2021, 26, 2959 17 of 35

Table A1. Cont.

Effects on Polyphenols Content and/or Food Processing Procedure Food Matrix Investigated Polyphenols Reference Antioxidant Activity Quercetin, kaempferol, caffeic All analyzed compounds decreased, with more severe Blanching 2.5 min at 96–98 ◦C acid, p-cumaric acid, sinapic decrease observed in the case of cooking. Kale leaves [68] and cooking 10 min at 100 ◦C acid, ferulic acid, total Antioxidant activity decreased by 32.6% in steamed, polyphenols and by 45.45% in cooked kale leaves. Boiling, steaming, and TPC Increased in all samples. microwaving (700 W) for 5, Eggplants (4 varieties) TPC [69] Antioxidant activity increased in all samples. 10, and 15 min Baking (the baked product Total polyphenols decreased but n.s. used 34 g of frozen Total polyphenols, total Total anthocyanins decreased significantly by 42.2% blueberries as a polyphenol anthocyanins, total Total procyanidins increased but n.s. source; the comparison was Blueberries procyanidins, quercetin, Quercetin increased but n.s. [76] carried out with a drink chlorogenic acid, caffeic acid, Chlorogenic acid increased significantly by 23.46% made by dissolving the same ferulic acid Caffeic acid increased but n.s. amount of frozen blueberries Ferulic acid increased but n.s. in water) Tomato-sauce production Phenolic acids decreased by 43.18% Phenolic acids, flavanones (cooking for 60 min at 99 ◦C Tomato Flavanones increased by 245.03% [73] and flavonols and crushing) Flavonols increased by 17.21% Total extractable polyphenols: increased by 152%, 236% and 164% after boiling, steaming and Boiling, steaming, and microwaving, respectively. Cassava Total extractable polyphenols [74] microwaving Antioxidant activity: increased by 151.56%, 208.60% and 173.44% after boiling, steaming and microwaving, respectively. TPC decreased by 29.63% and 45.68% after 4 months Sterilization until the and 12 months of storage, respectively. Runner bean TPC [70] temperature reached 123 ◦C Antioxidant activity decreased by 87.89% and 89.47% after 4 months and 12 months of storage, respectively. Molecules 2021, 26, 2959 18 of 35

Table A1. Cont.

Effects on Polyphenols Content and/or Food Processing Procedure Food Matrix Investigated Polyphenols Reference Antioxidant Activity TPC increased after almost all treatments and all varieties except in Beauregard from Croatia. TAC increased in all samples. Cooking in water (10 min), Sweet potatoes (2 TPC, TAC and phenolic acids chlorogenic acid decreased except after steaming in steaming (15 min, 97 ± 2 ◦C), varieties grown in (chlorogenic, neochlorogenic, Beauregard from Slovakia. [67] microwaving (5 min, 800 W), Slovakia and Croatia) and trans-ferulic) Neochlorogenic acid decreased in all samples. and baking (15 min, 200 ◦C) Trans-ferulic acid decreased in almost all samples except in boiled 414-purple from Croatia. Antioxidant activities increased in all samples. TAC decreased by 44.89% Canning in syrup with Cherries TAC Antioxidant capacity decreased by 33.03% measured by [78] thermal treatment FRAP assay. Trans-resveratrol and three All measured compounds (except genistein) decreased Canning in 5% brine Peanuts conjugates, caffeic acid, , [80] in all samples. genistein, quercetin and catechin TPC decreased by 13–47% in industrial setting and decrease by 2–33% in domestic setting Canning—industrial vs. TPC, procyanidins, phenolic Procyanidins decreased by 44% in industrial setting, Apricots [79] Canning domestic thermal processing acids and decreased by 2.4% in domestic setting Phenolic acids: higher decrease was observed in industrial vs. domestic cooking Chlorogenic acid increased by 31.31%, Neochlorogenic acid increased by 19.06%, Canning of apricot pulps, Catechin increased by 37.19%, followed by exhaustion Chlorogenic, neochlorogenic Kaempferol increased by 35.58%, under steam, and finally Apricots acid, catechin, kaempferol, [121] Quercetin increased by 26.08%, processed in an autoclave at quercetin, B2 Procyanidin B2 increased by 26.16% 121 ◦C for 30 min *The presented changes refer to only one variety, while two more varieties were used in the study. Molecules 2021, 26, 2959 19 of 35

Table A1. Cont.

Effects on Polyphenols Content and/or Food Processing Procedure Food Matrix Investigated Polyphenols Reference Antioxidant Activity Ellagic acid, gallic acid, ferulic acid, epicatechin and epigallocatechin were all affected by the treatments in the following order: canning yielded the highest content, followed by Ellagic acid, gallic acid, ferulic Canning vs. freezing freezing and drying (in all three varieties). Apricots acid, epicatechin, [122] (−18 ◦C) vs. drying (65 ◦C) Canning yielded the highest content in rutin, followed epigallocatechin, rutin by freezing and drying in one variety, while in other two varieties the rutin content was the highest in the case of canning, followed by drying then freezing. Neochlorogenic and chlorogenic acid and catechin— decreased (higher decrease after 55 ◦C). Neochlorogenic, chlorogenic Epicatechin, rutin and quercetin-3-0-glcoside— Drying at 55 and 75 ◦C Apricots (two cultivars) acid, catechin, epicatechin, rutin, [84] decreased (higher decrease after 75 ◦C). quercetin-3-O-glucoside Antioxidant activity increased in one variety with higher increase after 75 ◦C drying. Total content increased in yellow figs Drying (31–34 ◦C) for 8 days Figs (2 varieties) Total proanthocyanidin content And decreased in purple figs. [88] Antioxidant activity (ABTS, DPPH, and FRAP assays) decreased in both varieties. Drying TPC—FD gave the highest TPC, followed by air with sun exposure, without sun exposure, microwave-drying and finally convection-drying. Caffeic acid—FD gave the highest content, followed by Convection-oven-drying, air-drying with and then without sun, freeze-drying (FD), convection-oven-drying and microwave-drying. microwave-drying, and TPC, hydroxycinammic Spearmint Antioxidant activity: [123] air-drying with the sun acid derivatives FRAP—the highest value in FD sample, followed by exposure and without the air-drying with sun, without sun, convection-drying, sun exposure and microwave-drying; DPPH—the highest value in FD sample, followed by air-drying with sun, without sun, while microwave-and oven-drying gave similar values. Molecules 2021, 26, 2959 20 of 35

Table A1. Cont.

Effects on Polyphenols Content and/or Food Processing Procedure Food Matrix Investigated Polyphenols Reference Antioxidant Activity TPC—decreased by 37.33% after 65 ◦C, increased by 27.24% and 90.77% after 80 ◦C and FD, respectively. TAC—decreased by 38.46% and 66.67%, respectively, after 65 ◦C and 80 ◦C, and increased by 71.79% after FD. Convective hot-air-drying at TPC, TAC, gallic acid, catechin, Gallic acid increased in all samples 65 and 80 ◦C vs. Murtilla fruit quercetin-3-glucoside, , Catechin increased in 80 ◦C and FD, decreased in 65 ◦C [124] freeze-drying (FD) kaempferol, quercetin Quercetin 3-β-D-glucoside, myricetin, kaempferol— decreased in all samples Quercetin—increased in 65 ◦C and 80 ◦C, decreased in FD Antioxidant activity—increase in all samples Rutin apioside, rutin, naringenin , chlorogenic acid— decrease Naringenin—was not identified in raw, but it was in Drying (70 ◦C, 36 h) Tomatoes TPC, TFC [87] dried tomato Antioxidant activity—increase in antioxidant capacity (ABTS, DPPH, CUPRAC assays) Free —similar values in case of oven-drying and FD, bound and total phenols—higher values after Hot-air-oven-drying or oven-drying. Pumpkin flower Free, bound, total phenols [89] freeze-drying (FD) Antioxidant activity—hot-air-oven-dried pumpkin flours had slightly higher antioxidant activities than FD pumpkin flour samples. Drying at 60, 70, and 80 ◦C, respectively, at relative Maximum TPC at 70 ◦C, and it decreased with the humidity level of 50% for Cocoa beans TPC [85] increased drying time. heating time ranging from 0 to 40 h TPC decreased by 45% after drying at 40 ◦C. Drying at 40, 50, and 60 ◦C Cocoa beans TPC [83] Higher decrease with higher temperature. Molecules 2021, 26, 2959 21 of 35

Table A1. Cont.

Effects on Polyphenols Content and/or Food Processing Procedure Food Matrix Investigated Polyphenols Reference Antioxidant Activity Anthocyanins—FD preserved them the best, 130 ◦C drying degraded them. TPC—highest values obtained after 65 ◦C drying, Freeze-drying (FD), drying at followed by FD, 50 ◦C and 130 ◦C drying. 50 ◦C for 48 h, 65 ◦C for 20 h, Antioxidant activity: or 130 ◦C for 2 h until a Berries Anthocyanins (individual), TPC ABTS•+ radical scavenging activity and ferric-reducing [86] moisture 89 content below power varied depending on the berry type—raspberry 15% was obtained and boysenberry showed the highest ABTS in the case of 65◦C drying and redcurrant and blackcurrant in the case of FD, the same was observed for ferric-reducing power TPC decreased in all samples; the lowest decrease was observed in the lowest temperature regime and in the Vacuum/microwave-drying combined process. (480, 120 W), hot-air-drying Antioxidant activity decreased in ORAC values after (70, 60, 50 ◦C), and combined Jujube fruits (3 varieties) TPC drying, higher decrease in the case of higher [82] methods, such as pre-drying temperature; lower decrease in the case of and finish-drying microwave-drying. (60 ◦C + 480/120 W) Combined treatment gave lower decrease than hot-air-drying. Chlorogenic acid decreased by 16.02% Neochlorogenic acid decreased by 2.52% Catechin decreased by 3.66% Chlorogenic, neochlorogenic Kaempferol decreased by 9.20% Drying at 65 ◦C Apricots acid, catechin, kaempferol, [121] Quercetin decreased by 11.80% quercetin, procyanidin B2 Procyanidin B2 decreased by 14.57% *The presented changes refer to only one variety, while two more varieties were used in the study. Cold Processing Total phenolics, anthocyanins, Freezing at −30 ◦C Red Raspberries lambertianin C, sanguiin H-6, There was n.s. change in all analyzed compounds.[91] Freezing/ ellagic acid Chilling Individual TPC, total monomeric Berries There was n.s. change in all analyzed compounds. [94] quick-freezing process anthocyanins Molecules 2021, 26, 2959 22 of 35

Table A1. Cont.

Effects on Polyphenols Content and/or Food Processing Procedure Food Matrix Investigated Polyphenols Reference Antioxidant Activity Blanched/cooked kale TPC decreased by 3%. Freezing TPC [68] leaves Antioxidant activity decreased by 7% Cooling at 5 ◦C in the Polyphenol and anthocyanin Polyphenol and anthocyanin increased in both cases, refrigerator, or freezing at Maqui fruits [92] concentration with higher increase in the case of frozen samples. −20 ◦C TPC decreased before digestion in both Freezing by immersion at freezing methods. liquid nitrogen and Apples TPC [95] Antioxidant activity decreased before and after freeze-drying at −50 ◦C digestion (ABTS, CUPRAC, and FRAP assays). TPC and total monomeric anthocyanin content TPC and total monomeric Slow vs. quick freezing Strawberries increased in the case of quick-frozen samples compared [93] anthocyanin content with slow frozen samples. Chlorogenic acid increased by 6.55% Neochlorogenic acid increased by 1.08% Catechin increased by 17.69% Chlorogenic, neochlorogenic Kaempferol increased by 15.95% Deep-freezing to −18 ◦C Apricots acid, catechin, kaempferol, [121] Quercetin increased by 4.35% quercetin, procyanidin B2 Procyanidin B2 increased by 7.95% *The presented changes refer to only one variety, while two more varieties were used in the study. Compared with the freeze-dried snack: Freeze-drying vs. Infrared-drying caused important losses in most of the hot-air-drying vs. Phenolic acids, flavan-3-ols, apple (poly)phenolics infrared-drying vs. Red-fleshed apples flavonols, anthocyanins, Purée pasteurization maintained 65% the (poly)phenols [125] pasteurization of flavanones, dihydrochalcones Hot-air-drying maintained 83% the (poly)phenols apple puree) Anthocyanins were degraded to a higher extend after all thermal processing technologies. Biochemical Processing Red wine, dealcoholized M-3-G—red wine (68 mg), dealcoholized red wine Fermentation of red grape red wine, and red Malvidin-3-glucoside (M-3-G) [103] (58 mg) and red grape juice 117 mg grape juice Molecules 2021, 26, 2959 23 of 35

Table A1. Cont.

Effects on Polyphenols Content and/or Food Processing Procedure Food Matrix Investigated Polyphenols Reference Antioxidant Activity Eight cups of black tea (4 g tea solids) provided 108 µmol of quercetin glycosides (equivalent to 32.5 mg as free Black-tea fermentation Black vs. green tea Quercetin, kaempferol quercetin) and 72 µmol of kaempferol glycosides. The [105] green tea (4 g tea solids) provided 104 µmol of quercetin glycosides and 58 µmol of kaempferol glycosides per day. Fermentation (red-wine production)—comparison Total anthocyanin content was almost equal in both red Red grape Anthocyanins [102] between red wine and red grape juice and red wine. grape juice TPC decreased only in two varieties. Fermentation to apple cider Apple (5 varieties) TPC, catechin, caffeic acid Catechin increased in all varieties [101] Caffeic acid increased in two varieties Free soluble phenol content increased, Legumes—pigeon pea, Bound phenol content decreased bambara groundnut, Free and bound soluble Antioxidant activity: free soluble phenolic compounds of Natural fermentation [100] African yam bean, and phenol content fermented legumes had increased reducing power, free Fermentation kidney bean radical scavenging ability, and inhibition of lipid peroxidation compared with unfermented legumes. Eight legumes: black cow gram, mottled TPC increased in almost all samples Fermentation with naturally cowpea, speckled kidney Antioxidant activity increased in mottled cowpea, present bacteria and with TPC [99] bean, lentil, small rice speckled kidney bean and small rice bean, and n.s. changes lactic acid bacteria bean, small runner bean in all other samples. and two soya beans TPC—increase (more than 2-fold) Fermentation with Millet TPC Antioxidant activity (measured both by DPPH and ABTS [98] Aspergillus awamori assays)—slight increase by 3.75% and by 2.12% Ting fermentation (at All analyzed compounds—optimal values at 27 ◦C for 72 h TPC, total flavonoid and total different time and Sorghum Antioxidant activity—the best one was obtained in a [97] tannin content temperature regimes) sample fermented at 27 ◦C for 24 h Molecules 2021, 26, 2959 24 of 35

Table A1. Cont.

Effects on Polyphenols Content and/or Food Processing Procedure Food Matrix Investigated Polyphenols Reference Antioxidant Activity TPC: 34 and 37 mg of GAE 100 g−1 for, respectively, yogurt made with dates blended with milk and yogurt produced using small pieces of dates that were added Lactic acid fermentation Two types of yoghurt to milk. TPC and antioxidant activity [126] (milk enriched with dates) enriched with dates Antioxidant activity (measured by DDPH) was 51% and 57% for yogurt made with dates blended with milk and yogurt produced using small pieces of dates that were added to milk, respectively. Pickling (with variable The total free phenolic acids, the Total free phenolic acids increased. salinity and the addition of Potherb mustard total phenolic acids, total Total phenolics and total phenolic acids decreased. [127] Lactobacillus plantarum) phenolics Antioxidant activity decreased by 35%. TPC decreased by 68.40% Pickling Papaya TPC, TFC TFC decreased by 65.90% [128] Antioxidant activity (DDPH assay) decreased. TPC—after 15 days—decreased in all vegetable; after 30 and 60 days increased in all vegetables. Antioxidant activity: Green beans, green the Trolox equivalent antioxidant capacity decreased Pickling pepper, chili pepper, after 15 days, then increased after 30 and 60 days for white cabbage, Pickling TPC green beans, green pepper, chili pepper, cauliflower, [129] cauliflower, cucumber, white cabbage, cucumber and sneak melon. For tomato, sneak melon, tomato, carrot and it increased during all time points. carrot, garlic DPPH assay: RSA decreased followed by increase in all except green pepper, cauliflower, cucumber and sneak melon which decreased during all time points. TPC and TFC increased by 47% and 42%, respectively. TPC, TPA content, TFC, TPA decreased by 35% Pickling [130] naringenin, and Naringenin and vanillin increased (24 and 2.5-fold, respectively). Molecules 2021, 26, 2959 25 of 35

Table A1. Cont.

Effects on Polyphenols Content and/or Food Processing Procedure Food Matrix Investigated Polyphenols Reference Antioxidant Activity Mechanical Processing Peeling, trimming Flavonoids (quercetin Onions Flavonoids decreased by 39%. [108] and chopping and kaempferol) TPC—minor differences between the samples with and without the peel. Chlorogenic and neochlorogenic acid decreased in puree with peel (vs. puree without peels) Catechin increased in samples with peels (vs. puree TPC, chlorogenic, without peels). Removal of periderm Peaches neochlorogenic acid, catechin, Caffeic acid—slight decreased slightly in puree with [110] material in purée processing caffeic acid peels (vs. puree without peels). Peeling Antioxidant activity: Peach puree with periderm tissue that underwent blanching and pasteurization had 7–11% higher antioxidant activity (measured by beta-carotene/linoleic acid assay). Peeling Clingstone peaches TPC TPC decreased by 13–48% [111] Total polyphenol index increased especially in grapes Fermentation with Total polyphenol index, total with skins. Saccharomyces bayanus BC White grape [112] flavonoids Total flavonoids decreased in samples without skins, (with and without skins) while they increased in samples with skins. Catechins decreased in all analyzed catechins Superfine grinding (included Antioxidant activity increased in OH scavenging rate sieving through a 180 µm Green tea Catechins between the sample that was once sieved through a 180 [116] sieve once, or for 20–120 min) µm sieve and those that underwent sieving for 20–120 min.

Grinding Increase in luteolin-7-glucoside, umbelliferone, luteolin, 3,5-dicaffeoylquinic acid, and chlorogenic acid (the maximum values in the case of 180–315 and Grinding and sieving Hieracium pilosella L. Flavonoids and phenolic acids 315–500 µm). [114] Antioxidant activity increased in sieved samples (the maximum activity obtained at 180–315 and 315–500 µm). Molecules 2021, 26, 2959 26 of 35

Table A1. Cont.

Effects on Polyphenols Content and/or Food Processing Procedure Food Matrix Investigated Polyphenols Reference Antioxidant Activity TPC—the highest observed in the case of fine–coarse Grinding to produce powder. Further grinding decreased TPC. American, Turkish, and Coffee beans TPC Antioxidant activity—the highest observed in the case [115] Espresso coffees of fine–coarse powder. Further grinding decreased the antioxidant activity (DPPH assay). TPC increased (regardless of the particle size) Superfine grinding method Brazilian green propolis TPC Antioxidant activity increased (measured by ABTS and [117] DPPH, regardless of the particle size) Abbreviations: TPC—total phenolic content, TAC—total anthocyanin content, TPA—total phenolic acid content; TFC—total flavonoid content, HSTS—high-temperature short-time; PEF—pulsed electric field; sig—significant, n.s.—non significant; DPPH—2,2-diphenyl-1-picrylhydrazyl; ABTS—2,2’-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid; FRAP—ferric reducing antioxidant power; CUPRAC—cupric-reducing antioxidant capacity; GAE—gallic acid equivalent; RSA—radical scavenging activity.

Table A2. Overview of studies investigating the food-processing effects on polyphenols bioavailability/bioaccessibility.

Investigated Effects on Polyphenols on Food Processing Procedure Food Matrix Type of Study Reference Polyphenols Bioavailability/Bioaccessibility Plasma naringenin increased 2 h after consumption Cooking 15 min at Naringenin and In vivo crossover human Cherry tomato Plasma chlorogenic acid increased 2 and 6 h [72] 100 ◦C chlorogenic acid study on 5 subjects after consumption Acylation of anthocyanins: 11–14-fold decreased in Microwave (900 W) Acylated and anthocyanin recovery in urine and an 8–10-fold In vivo crossover human cooking for 12 or Purple carrots non-acylated decreased in anthocyanin recovery in plasma. [75] study, 12 subjects Heat treatment 20 min anthocyanin content Cooking increased the recovery of non-acylated anthocyanins but not acylated anthocyanins. Baking by using 34 g Total polyphenols, total AUC of phenolic metabolites were compared of frozen blueberries anthocyanins, total between baked product and blueberry as a polyphenol In vivo crossover human Blueberries procyanidins, quercetin, drink—increase in m-hydroxyphenylacetic, ferulic, [76] source and RCT, 10 subjects chlorogenic acid, caffeic isoferulic, and hydroxyhippuric acids and decrease comparison with acid, ferulic acid in hippuric, benzoic, salicylic, and sinapic acids. blueberry drink. Molecules 2021, 26, 2959 27 of 35

Table A2. Cont.

Investigated Effects on Polyphenols on Food Processing Procedure Food Matrix Type of Study Reference Polyphenols Bioavailability/Bioaccessibility Tomato sauce production (boiling Phenolic acids, In vivo crossover human Increase of plasma concentration and urinary Tomato [73] for 60 min at 99 ◦C flavanones and flavonols RCT with 8 subjects excretion of naringenin glucuronide. and crushing) Bioaccessability of total phenolic acids decreased by 12.70% compared with the control sample Orange, kiwi, Thermal treatment at Total phenolic acids, In vitro gastrointestinal Bioaccessability of total flavonoids increased by pineapple and [131] 90 ◦C for 60 s total flavonoids, TPC digestion model 2.65% compared with the control sample mango juices Bioaccessability of TPC decreased by 4.17% compared with the control sample Bioaccessibility of total polyphenols in heated apple juices did not change compared to the control juice. Bioaccessibility of total polyphenols in grape juice Heating at 80 and Apple, orange and In vitro gastrointestinal increased by 33.9% and 27.3% for those treated at 80 Total Polyphenols [132] 90 ◦C for 30 s grape juice digestion model and 90 ◦C, respectively. Bioaccessibility of total polyphenols in increased by 19% and 29.2% for samples heated at 80 and 80 ◦C, respectively. Bioaccessability for total extractable polyphenols was 72.94% after boiling, 74.54% after steaming, and Boiling, steaming, Total extractable In vitro gastrointestinal 72.67% after microwaving Cassava [74] microwaving polyphenols digestion model Bioaccessability for antioxidative activity was 34.78% after boiling, 36.71% after steaming and 36.85% after microwaving In vitro simulated Increase in bioaccessibility of total Drying (31–34 ◦C) for Total proanthocyani- Figs (2 varieties) gastrointestinal proanthocyanidins and chlorogenic acid content and [88] 8 days din content digestion model decrease in anthocyanin bioaccessibility. In vitro gastrointestinal Compared with raw tomatoes, dried tomatoes had Drying (70 ◦C, 36 h) Tomatoes TPC, TFC [87] Drying digestion model higher TPC and TFC values during digestion. In vitro digestion Hot-air-oven-drying Free, bound, total Phenolic bioaccessibility for oven-dried sample was Pumpkin flower enzymatic extraction [89] or Freeze-drying phenols 30.76% and for freeze-drying it was 29.19%. method Molecules 2021, 26, 2959 28 of 35

Table A2. Cont.

Investigated Effects on Polyphenols on Food Processing Procedure Food Matrix Type of Study Reference Polyphenols Bioavailability/Bioaccessibility Freeze-drying vs. hot-air-drying vs. Percentage of urine excretion of total polyphenols infrared-drying (35, In vivo human crossover was the highest in the case of pasteurized puree, Apples puree Total polyphenols [125] 40, 50, and 60 ◦C) vs. study, 3 subjects followed by hot-air-dried and then pasteurization of freeze-dried samples. apple puree Freezing by immersion at liquid In vitro gastric digestion Decrease in TPC during and after digestion with nitrogen and Apples TPC [95] model both freezing methods. freeze-drying at −50 ◦C Freezing Overall, after the completion of in vitro digestion, Individual quick bioaccessibility values for TPC, TFC, TMAC, and freezing (IQF) and In vitro gastric digestion TAC were found to be 94–105%, 64–91%, 47–83%, Strawberries TPC, TFC, TAC, TMAC [133] conventional model and 55–84%, respectively. TMAC from frozen freezing (CF) strawberries was significantly more bioaccessible than that of fresh strawberries (P < 0.05). Red wine, Fermentation of dealcoholized red Malvidin-3-glucoside In vivo, crossover The plasma levels of M-3-G was similar between all [103] red grape wine and red (M-3-G) human RCT, 6 subjects three arms. grape juice Black tea In vivo human study, 18 Quercetin and kaempferol plasma levels showed no Black vs. green tea Quercetin, kaempferol [105] fermentation subjects difference between the two tea types. Fermentation Total dietary anthocyanins—higher bioavailability of those from red grape juice compared to those in red wine. Fermentation of red Wine vs. red Acute in vivo human Low urinary excretion of dietary anthocyanins with wine and red Anthocyanins [102] grape juice study, 9 subjects values below 1%. Only 0.25% and 0.18% of the grape juice administered dose of total anthocyanins was excreted within 7 h after red grape juice and red wine ingestion, respectively. Molecules 2021, 26, 2959 29 of 35

Table A2. Cont.

Investigated Effects on Polyphenols on Food Processing Procedure Food Matrix Type of Study Reference Polyphenols Bioavailability/Bioaccessibility A total of 24 Bioavailability of phenolic metabolites in urine in (poly)phenol metabolites Controlled alcoholic In vivo human crossover comparison with total intake of polyphenols was Orange juice including both flavanone [134] fermentation study, 9 subjects lower in fermented orange juice (around 46%) than and phenolic acid in orange juice (59%). derivatives Abbreviations: TPC—total phenolic content, TAC—total anthocyanin content, TPA—total phenolic acid content; TFC—total flavonoid content, RCT—randomized controlled trial, AUC—area under the ROC curve, M-3-G—malvidin-3-glucoside, FD—freeze-drying, TMAC—total monomeric anthocyanin content. Molecules 2021, 26, 2959 30 of 35

References 1. Duncan, M.J.; Kline, C.E.; Vandelanotte, C.; Sargent, C.; Rogers, N.L.; Di Milia, L. Cross-sectional associations between multiple lifestyle behaviors and health-related quality of life in the 10,000 Steps cohort. PLoS ONE 2014, 9, e94184. [CrossRef] 2. Tomás-Barberán, F.A.; Andrés-Lacueva, C. Polyphenols and health: Current state and progress. J. Agric. Food Chem. 2012, 60, 8773–8775. [CrossRef] 3. Afanas’ev, I.B.; Dcrozhko, A.I.; Brodskii, A.V.; Kostyuk, V.A.; Potapovitch, A.I. Chelating and free radical scavenging mechanisms of inhibitory action of rutin and quercetin in lipid peroxidation. Biochem. Pharmacol. 1989, 38, 1763–1769. [CrossRef] 4. Cory, H.; Passarelli, S.; Szeto, J.; Tamez, M.; Mattei, J. The Role of Polyphenols in Human Health and Food Systems: A Mini-Review. Front. Nutr. 2018, 5, 87. [CrossRef] 5. Caballero, B.; Allen, L.; Prentice, A. Encyclopedia of , 2nd ed.; Academic Press: Cambridge, MA, USA, 2005; pp. 150–300. 6. Koli, R.; Erlund, I.; Jula, A.; Marniemi, J.; Mattila, P.; Alfthan, G. Bioavailability of Various Polyphenols from a Diet Containing Moderate Amounts of Berries. J. Agric. Food Chem. 2010, 58, 3927–3932. [CrossRef] 7. Ifie, I.; Marshall, L.J.; Yildiz, F. Food processing and its impact on phenolic constituents in food. Cogent Food Agric. 2018, 4, 1507782. [CrossRef] 8. Jiménez-Monreal, A.M.; García-Diz, L.; Martínez-Tomé, M.; Mariscal, M.; Murcia, M.A. Influence of cooking methods on antioxidant activity of vegetables. J. Food Sci. 2009, 74, H97–H103. [CrossRef][PubMed] 9. Nayak, B.; Liu, R.H.; Tang, J. Effect of Processing on Phenolic Antioxidants of Fruits, Vegetables, and Grains—A Review. Crit. Rev. Food Sci. Nutr. 2015, 55, 887–918. [CrossRef][PubMed] 10. D’Archivio, M.; Filesi, C.; Varì, R.; Scazzocchio, B.; Masella, R. Bioavailability of the polyphenols: Status and controversies. Int. J. Mol. Sci. 2010, 11, 1321–1342. [CrossRef][PubMed] 11. Tsao, R. Chemistry and biochemistry of dietary polyphenols. Nutrients 2010, 2, 1231–1246. [CrossRef][PubMed] 12. Haminiuk, C.W.I.; Maciel, G.M.; Plata-Oviedo, M.S.V.; Peralta, R.M. Phenolic compounds in fruits—An overview. Int. J. Food Sci. Technol. 2012, 47, 2023–2044. [CrossRef] 13. Amarowicz, R.; Carle, R.; Dongowski, G.; Durazzo, A.; Galensa, R.; Kammerer, D.; Maiani, G.; Piskula, M.K. Influence of postharvest processing and storage on the content of phenolic acids and flavonoids in foods. Mol. Nutr Food Res. 2009, 53, S151–S183. [CrossRef][PubMed] 14. Crozier, A.; Del Rio, D.; Clifford, M.N. Bioavailability of dietary flavonoids and phenolic compounds. Mol. Aspects Med. 2010, 31, 446–467. [CrossRef][PubMed] 15. Williams, C.A. Flavone and flavonol O-glycosides. In Flavonoids: Chemistry, Biochemistry and Applications; Andersen, O.M., Markham, K.R., Eds.; CRC Press: Boca Raton, FL, USA, 2006; pp. 749–856. 16. Quideau, S. Flavonoids. Chemistry, Biochemistry and Applications; Andersen, Ø.M., Markham, K.R., Eds.; Wiley Online Library: Hoboken, NJ, USA, 2006. [CrossRef] 17. Cardozo, L.F.; Pedruzzi, L.M.; Stenvinkel, P.; Stockler-Pinto, M.B.; Daleprane, J.B.; Leite, M., Jr.; Mafra, D. Nutritional strategies to modulate inflammation and oxidative stress pathways via activation of the master antioxidant switch Nrf2. Biochimie 2013, 95, 1525–1533. [CrossRef] 18. Siriwardhana, N.; Kalupahana, N.S.; Cekanova, M.; LeMieux, M.; Greer, B.; Moustaid-Moussa, N. Modulation of adipose tissue inflammation by bioactive food compounds. J. Nutr. Biochem. 2013, 24, 613–623. [CrossRef] 19. Wang, S.; Moustaid-Moussa, N.; Chen, L.; Mo, H.; Shastri, A.; Su, R.; Bapat, P.; Kwun, I.S.; Shen, C.L. Novel insights of dietary polyphenols and obesity. J. Nutr. Biochem. 2014, 25, 1–18. [CrossRef] 20. Bose, M.; Lambert, J.D.; Ju, J.; Reuhl, K.R.; Shapses, S.A.; Yang, C.S. The major green tea polyphenol, (-)-epigallocatechin-3-gallate, inhibits obesity, metabolic syndrome, and fatty liver disease in high-fat-fed mice. J. Nutr. 2008, 138, 1677–1683. [CrossRef] 21. Isaak, C.K.; Petkau, J.C.; Blewett, H.; Karmin, O.; Siow, Y.L. Lingonberry anthocyanins protect cardiac cells from oxidative-stress- induced apoptosis. Can. J. Physiol. Pharmacol. 2017, 95, 904–910. [CrossRef][PubMed] 22. Rossi, A.; Serraino, I.; Dugo, P.; Di Paola, R.; Mondello, L.; Genovese, T.; Morabito, D.; Dugo, G.; Sautebin, L.; Caputi, A.P.; et al. Protective effects of anthocyanins from blackberry in a rat model of acute lung inflammation. Free Radic. Res. 2003, 37, 891–900. [CrossRef] 23. Lee, M.; Sorn, S.R.; Park, Y.; Park, H.K. Anthocyanin rich-black soybean testa improved visceral fat and plasma lipid profiles in overweight/obese Korean adults: A randomized controlled trial. J. Med. Food 2016, 19, 995–1003. [CrossRef] 24. Silveira, J.Q.; Dourado, G.K.Z.S.; Cesar, T.B. Red-fleshed sweet orange juice improves the risk factors for metabolic syndrome. Int. J. Food Sci. Nutr. 2015, 66, 830–836. [CrossRef] 25. Fisher, N.D.L.; Hughes, M.; Gerhard-Herman, M.; Hollenberg, N.K. Flavanol-rich cocoa induces nitric-oxide-dependent vasodila- tion in healthy humans. J. Hypertens. 2003, 21, 2281–2286. [CrossRef] 26. Argani, H.; Ghorbanihaghjo, A.; Vatankhahan, H.; Rashtchizadeh, N.; Raeisi, S.; Ilghami, H. The effect of red grape seed extract on serum paraoxonase activity in patients with mild to moderate hyperlipidemia. Sao Paulo Med. J. 2016, 134, 234–239. [CrossRef] [PubMed] Molecules 2021, 26, 2959 31 of 35

27. Brüll, V.; Burak, C.; Stoffel-Wagner, B.; Wolffram, S.; Nickenig, G.; Müller, C.; Langguth, P.; Alteheld, B.; Fimmers, R.; Naaf, S.; et al. Effects of a quercetin-rich onion skin extract on 24 h ambulatory blood pressure and endothelial function in overweight-to-obese patients with (pre-)hypertension: A randomised double-blinded placebo-controlled cross-over trial. Br. J. Nutr. 2015, 114, 1263–1277. [CrossRef] 28. Choi, E.Y.; Lee, H.; Woo, J.S.; Jang, H.H.; Hwang, S.J.; Kim, H.S.; Kim, W.S.; Kim, Y.S.; Choue, R.; Cha, Y.J.; et al. Effect of onion peel extract on endothelial function and endothelial progenitor cells in overweight and obese individuals. Nutrition 2015, 31, 1131–1135. [CrossRef][PubMed] 29. Potì, F.; Santi, D.; Spaggiari, G.; Zimetti, F.; Zanotti, I. Polyphenol health effects on cardiovascular and neurodegenerative disorders: A review and meta-analysis. Int. J. Mol. Sci. 2019, 20, 351. [CrossRef][PubMed] 30. Hanhineva, K.; Törrönen, R.; Bondia-Pons, I.; Pekkinen, J.; Kolehmainen, M.; Mykkänen, H.; Poutanen, K. Impact of dietary polyphenols on carbohydrate metabolism. Int. J. Mol. Sci. 2010, 11, 1365–1402. [CrossRef] 31. Rienks, J.; Barbaresko, J.; Oluwagbemigun, K.; Schmid, M.; Nöthlings, U. Polyphenol exposure and risk of type 2 diabetes: Dose-response meta-analyses and systematic review of prospective cohort studies. Am. J. Clin. Nutr. 2018, 108, 49–61. [CrossRef] [PubMed] 32. Yang, W.S.; Wang, W.Y.; Fan, W.Y.; Deng, Q.; Wang, X. Tea consumption and risk of type 2 diabetes: A dose-response meta-analysis of cohort studies. Br. J. Nutr. 2014, 111, 1329–1339. [CrossRef][PubMed] 33. Wang, P.Y.; Fang, J.C.; Gao, Z.H.; Zhang, C.; Xie, S.Y. Higher intake of fruits, vegetables or their fiber reduces the risk of type 2 diabetes: A meta-analysis. J. Diabetes Investig. 2016, 7, 56–69. [CrossRef] 34. Gowd, V.; Xie, L.; Sun, C.; Chen, W. Phenolic profile of bayberry followed by simulated gastrointestinal digestion and gut microbiota fermentation and its antioxidant potential in HepG2 cells. J. Funct. Foods 2020, 70, 103987. [CrossRef] 35. Briguglio, G.; Costa, C.; Pollicino, M.; Giambò, F.; Catania, S.; Fenga, C. Polyphenols in cancer prevention: New insights (Review). Int. J. Funct. Nutr. 2020, 1, 9. [CrossRef] 36. Christensen, K.Y.; Naidu, A.; Parent, M.É.; Pintos, J.; Abrahamowicz, M.; Siemiatycki, J.; Koushik, A. The risk of lung cancer related to dietary intake of flavonoids. Nutr. Cancer 2012, 64, 964–974. [CrossRef][PubMed] 37. Woo, H.D.; Lee, J.; Choi, I.J.; Kim, C.G.; Lee, J.Y.; Kwon, O.; Kim, J. Dietary flavonoids and gastric cancer risk in a Korean population. Nutrients 2014, 6, 4961–4973. [CrossRef][PubMed] 38. Hoensch, H.; Groh, B.; Edler, L.; Kirch, W. Prospective cohort comparison of flavonoid treatment in patients with resected colorectal cancer to prevent recurrence. World J. Gastroenterol. 2008, 14, 2187–2193. [CrossRef][PubMed] 39. Zhang, G.; Wang, Y.; Zhang, Y.; Wan, X.; Li, J.; Liu, K.; Wang, F.; Liu, Q.; Yang, C.; Yu, P.; et al. Anti-Cancer Activities of Tea Epigallocatechin-3-Gallate in Breast Cancer Patients under Radiotherapy. Curr. Mol. Med. 2012, 12, 163–176. [CrossRef][PubMed] 40. Grosso, G.; Micek, A.; Marranzano, M.; Mistretta, A.; Giovannucci, E.L. Dietary polyphenols and cancer incidence: A comprehen- sive meta-analysis. Eur. J. Public Health 2015, 25, ckv175.177. [CrossRef] 41. Flanagan, E.; Müller, M.; Hornberger, M.; Vauzour, D. Impact of Flavonoids on Cellular and Molecular Mechanisms Underlying Age-Related Cognitive Decline and Neurodegeneration. Curr. Nutr. Rep. 2018, 7, 49–57. [CrossRef][PubMed] 42. Bell, L.; Lamport, D.J.; Butler, L.T.; Williams, C.M. A review of the cognitive effects observed in humans following acute supplementation with flavonoids, and their associated mechanisms of action. Nutrients 2015, 7, 10290–10306. [CrossRef] 43. Evans, H.M.; Howe, P.R.C.; Wong, R.H.X. Effects of resveratrol on cognitive performance, mood and cerebrovascular function in post-menopausal women; A 14-week randomised placebo-controlled intervention trial. Nutrients 2017, 9, 27. [CrossRef] [PubMed] 44. Heaney, R.P. Factors influencing the measurement of bioavailability, taking calcium as a model. J. Nutr. 2001, 131, 1344S–1348S. [CrossRef] 45. Ribas-Agustí, A.; Martín-Belloso, O.; Soliva-Fortuny, R.; Elez-Martínez, P. Food processing strategies to enhance phenolic compounds bioaccessibility and bioavailability in plant-based foods. Crit. Rev. Food Sci. Nutr. 2018, 58, 2531–2548. [CrossRef] [PubMed] 46. Holst, B.; Williamson, G. Nutrients and : From bioavailability to bioefficacy beyond antioxidants. Curr. Opin. Biotechnol. 2008, 19, 73–82. [CrossRef][PubMed] 47. Courraud, J.; Berger, J.; Cristol, J.P.; Avallone, S. Stability and bioaccessibility of different forms of and A during in vitro digestion. Food Chem. 2013, 136, 871–877. [CrossRef][PubMed] 48. Rein, M.J.; Renouf, M.; Cruz-Hernandez, C.; Actis-Goretta, L.; Thakkar, S.K.; da Silva Pinto, M. Bioavailability of bioactive food compounds: A challenging journey to bioefficacy. Br. J. Clin. Pharmacol. 2013, 75, 588–602. [CrossRef] 49. Carbonell-Capella, J.M.; Buniowska, M.; Barba, F.J.; Esteve, M.J.; Frígola, A. Analytical methods for determining bioavailability and bioaccessibility of bioactive compounds from fruits and vegetables: A review. Compr. Rev. Food Sci. Food Saf. 2014, 13, 155–171. [CrossRef][PubMed] 50. Manach, C.; Scalbert, A.; Morand, C.; Rémésy, C.; Jiménez, L. Polyphenols: Food sources and bioavailability. Am. J. Clin. Nutr. 2004, 79, 727–747. [CrossRef] 51. Aura, A.-M.; Martin-Lopez, P.; O’Leary, K.A.; Williamson, G.; Oksman-Caldentey, K.-M.; Poutanen, K.; Santos-Buelga, C. In vitro metabolism of anthocyanins by human gut microflora. Eur. J. Nutr. 2005, 44, 133–142. [CrossRef] 52. Day, A.J.; Bao, Y.; Morgan, M.R.; Williamson, G. Conjugation position of quercetin glucuronides and effect on biological activity. Free Radic. Biol. Med. 2000, 29, 1234–1243. [CrossRef] Molecules 2021, 26, 2959 32 of 35

53. Inada, K.O.P.; Silva, T.B.R.; Lobo, L.A.; Domingues, R.M.C.P.; Perrone, D.; Monteiro, M. Bioaccessibility of phenolic compounds of jaboticaba (Plinia jaboticaba) peel and seed after simulated gastrointestinal digestion and gut microbiota fermentation. J. Funct. Foods 2020, 67, 103851. [CrossRef] 54. Karakaya, S. Bioavailability of Phenolic Compounds. Crit. Rev. Food Sci. Nutr. 2004, 44, 453–464. [CrossRef] 55. Prior, R.L.; Wu, X. Anthocyanins: Structural characteristics that result in unique metabolic patterns and biological activities. Free Radic. Res. 2006, 40, 1014–1028. [CrossRef][PubMed] 56. Hollands, W.; Brett, G.M.; Radreau, P.; Saha, S.; Teucher, B.; Bennett, R.N.; Kroon, P.A. Processing blackcurrants dramatically reduces the content and does not enhance the urinary yield of anthocyanins in human subjects. Food Chem. 2008, 108, 869–878. [CrossRef][PubMed] 57. Kahle, K.; Huemmer, W.; Kempf, M.; Scheppach, W.; Erk, T.; Richling, E. Polyphenols are intensively metabolized in the human gastrointestinal tract after apple juice consumption. J. Agric. Food Chem. 2007, 55, 10605–10614. [CrossRef][PubMed] 58. Serrano, J.; Puupponen-Pimiä, R.; Dauer, A.; Aura, A.M.; Saura-Calixto, F. Tannins: Current knowledge of food sources, intake, bioavailability and biological effects. Mol. Nutr. Food Res. 2009, 53, S310–S329. [CrossRef][PubMed] 59. Pandey, K.B.; Rizvi, S.I. Plant polyphenols as dietary antioxidants in human health and disease. Oxid. Med. Cell. Longev. 2009, 2, 270–278. [CrossRef] 60. Rothwell, J.A.; Medina-Remón, A.; Pérez-Jiménez, J.; Neveu, V.; Knaze, V.; Slimani, N.; Scalbert, A. Effects of food processing on polyphenol contents: A systematic analysis using Phenol-Explorer data. Mol. Nutr. Food Res. 2015, 59, 160–170. [CrossRef] [PubMed] 61. Peleg, H.; Naim, M.; Rouseff, R.L.; Zehavi, U. Distribution of bound and free phenolic acids in oranges (Citrus sinensis) and (Citrus paradisi). J. Sci. Food Agric. 1991, 57, 417–426. [CrossRef] 62. Minatel, I.O.; Borges, C.V.; Ferreira, M.I.; Gomez, H.A.G.; Chen, C.-Y.O.; Lima, G.P.P. Phenolic Compounds: Functional Properties, Impact of Processing and Bioavailability. Phenolic Compd. Biol. Act. 2017.[CrossRef] 63. Miglio, C.; Chiavaro, E.; Visconti, A.; Fogliano, V.; Pellegrini, N. Effects of different cooking methods on nutritional and physicochemical characteristics of selected vegetables. J. Agric. Food Chem. 2008, 56, 139–147. [CrossRef] 64. Makris, D.P.; Rossiter, J.T. Domestic processing of onion bulbs (Allium cepa) and asparagus spears (Asparagus officinalis): Effect on flavonol content and antioxidant status. J. Agric. Food Chem. 2001, 49, 3216–3222. [CrossRef][PubMed] 65. Rodrigues, A.S.; Pérez-Gregorio, M.R.; García-Falcón, M.S.; Simal-Gándara, J. Effect of curing and cooking on flavonols and anthocyanins in traditional varieties of onion bulbs. Food Res. Int. 2009, 42, 1331–1336. [CrossRef] 66. Andlauer, W.; Stumpf, C.; Hubert, M.; Rings, A.; Fürst, P. Influence of cooking process on phenolic marker compounds of vegetables. Int. J. Vitam. Nutr. Res. 2003, 73, 152–159. [CrossRef] 67. Musilova, J.; Lidikova, J.; Vollmannova, A.; Frankova, H.; Urminska, D.; Bojnanska, T.; Toth, T. Influence of Heat Treatments on the Content of Bioactive Substances and Antioxidant Properties of Sweet Potato (Ipomoea batatas L.) Tubers. J. Food Qual. 2020, 2020, 8856260. [CrossRef] 68. Korus, A.; Lisiewska, Z. Effect of preliminary processing and method of preservation on the content of selected antioxidative compounds in kale (Brassica oleracea L. var. acephala) leaves. Food Chem. 2011, 129, 149–154. [CrossRef] 69. Chumyam, A.; Whangchai, K.; Jungklang, J.; Faiyue, B.; Saengnil, K. Effects of heat treatments on antioxidant capacity and total phenolic content of four cultivars of purple skin eggplants. ScienceAsia 2013, 39, 246–251. [CrossRef] 70. Wołosiak, R.; Druzynska, B.; Piecyk, M.; Majewska, E.; Worobiej, E. Effect of sterilization process and storage on the antioxidative properties of runner bean. Molecules 2018, 23, 1409. [CrossRef][PubMed] 71. Aguilar-Rosas, S.F.; Ballinas-Casarrubias, M.L.; Nevarez-Moorillon, G.V.; Martin-Belloso, O.; Ortega-Rivas, E. Thermal and pulsed electric fields pasteurization of apple juice: Effects on physicochemical properties and flavour compounds. J. Food Eng. 2007, 83, 41–46. [CrossRef] 72. Bugianesi, R.; Salucci, M.; Leonardi, C.; Ferracane, R.; Catasta, G.; Azzini, E.; Maiani, G. Effect of domestic cooking on human bioavailability of naringenin, chlorogenic acid, lycopene and β-carotene in cherry tomatoes. Eur. J. Nutr. 2004, 43, 360–366. [CrossRef] 73. Martínez-Huélamo, M.; Tulipani, S.; Estruch, R.; Escribano, E.; Illán, M.; Corella, D.; Lamuela-Raventós, R.M. The tomato sauce making process affects the bioaccessibility and bioavailability of tomato phenolics: A pharmacokinetic study. Food Chem. 2015, 173, 864–872. [CrossRef] 74. De Lima, A.C.S.; da Rocha Viana, J.D.; de Sousa Sabino, L.B.; da Silva, L.M.R.; da Silva, N.K.V.; de Sousa, P.H.M. Processing of three different cooking methods of cassava: Effects on in vitro bioaccessibility of phenolic compounds and antioxidant activity. LWT Food Sci. Technol. 2017, 76, 253–258. [CrossRef] 75. Kurilich, A.C.; Clevidence, B.A.; Britz, S.J.; Simon, P.W.; Novotny, J.A. Plasma and urine responses are lower for acylated vs nonacylated anthocyanins from raw and cooked purple carrots. J. Agric. Food Chem. 2005, 53, 6537–6542. [CrossRef] 76. Rodriguez-Mateos, A.; del Pino-García, R.; George, T.W.; Vidal-Diez, A.; Heiss, C.; Spencer, J.P.E. Impact of processing on the bioavailability and vascular effects of blueberry (poly)phenols. Mol. Nutr. Food Res. 2014, 58, 1952–1961. [CrossRef][PubMed] 77. Vergara-Balderas, F.T. Canning: Process of Canning. In Encyclopedia of Food and Health; Caballero, B., Finglas, P.M., Toldra, F., Eds.; Elsevier Inc.: Amsterdam, The Netherlands, 2016; pp. 628–632. 78. Chaovanalikit, A.; Wrolstad, R.E. Anthocyanin and Polyphenolic Composition of Fresh and Processed Cherries. J. Food Sci. 2004, 69, FCT73–FCT83. [CrossRef] Molecules 2021, 26, 2959 33 of 35

79. Le Bourvellec, C.; Gouble, B.; Bureau, S.; Reling, P.; Bott, R.; Ribas-Agusti, A.; Audergon, J.M.; Renard, C.M.G.C. Impact of canning and storage on apricot carotenoids and polyphenols. Food Chem. 2018, 240, 615–625. [CrossRef][PubMed] 80. Chukwumah, Y.; Walker, L.; Ogutu, S.; Wambura, P.; Verghese, M. Effect of canning and storage on the phenolic composition of peanuts. J. Food Process. Preserv. 2013, 37, 582–588. [CrossRef] 81. Sontakke, M.S.; Salve, S.P. Solar Drying Technologies: A Review. Int. Refereed J. Eng. Sci. 2015, 4, 29–35. 82. Wojdyło, A.; Lech, K.; Nowicka, P.; Hernandez, F.; Figiel, A.; Carbonell-Barrachina, A.A. Influence of different drying techniques on phenolic compounds, antioxidant capacity and colour of ziziphus jujube mill. Fruits. Molecules 2019, 24, 2361. [CrossRef] [PubMed] 83. Alean, J.; Chejne, F.; Rojano, B. Degradation of polyphenols during the cocoa drying process. J. Food Eng. 2016, 189, 99–105. [CrossRef] 84. Madrau, M.A.; Piscopo, A.; Sanguinetti, A.M.; Del Caro, A.; Poiana, M.; Romeo, F.V.; Piga, A. Effect of drying temperature on polyphenolic content and antioxidant activity of apricots. Eur. Food Res. Technol. 2009, 228, 441–448. [CrossRef] 85. Abhay, S.; Hii, C.; Law, C.; Suzannah, S.; Djaeni, M. Effect of hot-air drying temperature on the polyphenol content and the sensory properties of cocoa beans. Int. Food Res. J. 2016, 23, 1479–1484. 86. Bustos, M.C.; Rocha-Parra, D.; Sampedro, I.; De Pascual-Teresa, S.; León, A.E. The Influence of Different Air-Drying Conditions on Bioactive Compounds and Antioxidant Activity of Berries. J. Agric. Food Chem. 2018, 66, 2714–2723. [CrossRef] 87. Kamiloglu, S.; Demirci, M.; Selen, S.; Toydemir, G.; Boyacioglu, D.; Capanoglu, E. Home processing of tomatoes (Solanum lycopersicum): Effects on in vitro bioaccessibility of total lycopene, phenolics, flavonoids, and antioxidant capacity. J. Sci. Food Agric. 2014, 94, 2225–2233. [CrossRef] 88. Kamiloglu, S.; Capanoglu, E. Investigating the in vitro bioaccessibility of polyphenols in fresh and sun-dried figs ( carica L.). Int. J. Food Sci. Technol. 2013, 48, 2621–2629. [CrossRef] 89. Aydin, E.; Gocmen, D. The influences of drying method and metabisulfite pre-treatment onthe color, functional properties and phenolic acids contents and bioaccessibility of pumpkin flour. LWT Food Sci. Technol. 2015, 60, 385–392. [CrossRef] 90. Tucker, G.S. Food Biodeterioration and Preservation; Blackwell Publishing: Hoboken, NJ, USA, 2008; pp. 81–135. 91. Mullen, W.; Stewart, A.J.; Lean, M.E.J.; Gardner, P.; Duthie, G.G.; Crozier, A. Effect of freezing and storage on the phenolics, , flavonoids, and antioxidant capacity of red raspberries. J. Agric. Food Chem. 2002, 50, 5197–5201. [CrossRef] [PubMed] 92. González, B.; Vogel, H.; Razmilic, I.; Wolfram, E. Polyphenol, anthocyanin and antioxidant content in different parts of maqui fruits (Aristotelia chilensis) during ripening and conservation treatments after harvest. Ind. Crop. Prod. 2015, 76, 158–165. [CrossRef] 93. Yanat, M.; Baysal, T. Effect of freezing rate and storage time on quality parameters of frozen in modified and home type freezer. Hrvat. Cas.ˇ Prehrambenu Tehnol. Biotehnol. Nutr. 2018, 13, 154–158. [CrossRef] 94. Poiana, M.A.; Moigradean, D.; Raba, D.; Aida, L.M.; Popa, M. The effect of long-term frozen storage on the nutraceutical compounds, antioxidant properties and color indices of different kinds of berries. J. Food Agric. Environ. 2010, 1, 54–58. 95. Dalmau, M.E.; Bornhorst, G.M.; Eim, V.; Rosselló, C.; Simal, S. Effects of freezing, freeze drying and convective drying on in vitro gastric digestion of apples. Food Chem. 2017, 215, 7–16. [CrossRef] 96. Van Boekel, M.; Fogliano, V.; Pellegrini, N.; Stanton, C.; Scholz, G.; Lalljie, S.; Somoza, V.; Knorr, D.; Jasti, P.R.; Eisenbrand, G. A review on the beneficial aspects of food processing. Mol. Nutr. Food Res. 2010, 54, 1215–1247. [CrossRef] 97. Adebo, O.A.; Njobeh, P.B.; Adebiyi, J.A.; Kayitesi, E. Co-influence of fermentation time and temperature on physicochemical properties, bioactive components and microstructure of ting (a Southern African food) from whole grain sorghum. Food Biosci. 2018, 25, 118–127. [CrossRef] 98. Salar, R.K.; Purewal, S.S.; Bhatti, M.S. Optimization of extraction conditions and enhancement of phenolic content and antioxidant activity of pearl millet fermented with Aspergillus awamori MTCC-548. Resour. Effic. Technol. 2016, 2, 148–157. [CrossRef] 99. Gan, R.-Y.; Shah, N.P.; Wang, M.-F.; Lui, W.-Y.; Corke, H. Fermentation alters antioxidant capacity and polyphenol distribution in selected edible legumes. Int. J. Food Sci. Technol. 2016, 51, 875–884. [CrossRef] 100. Oboh, G.; Ademiluyi, A.O.; Akindahunsi, A.A. Changes in Polyphenols Distribution and Antioxidant Activity during Fermenta- tion of Some Underutilized Legumes. Food Sci. Technol. Int. 2009, 15, 41–46. [CrossRef] 101. Nogueira, A.; Guyot, S.; Marnet, N.; Lequéré, J.M.; Drilleau, J.F.; Wosiacki, G. Effect of alcoholic fermentation in the content of phenolic compounds in cider processing. Braz. Arch. Biol. Technol. 2008, 51, 1025–1032. [CrossRef] 102. Frank, T.; Netzel, M.; Strass, G.; Bitsch, R.; Bitsch, I. Bioavailability of -3- following consumption of red wine and red grape juice. Can. J. Physiol. Pharmacol. 2003, 81, 423–435. [CrossRef] 103. Bub, A.; Watzl, B.; Heeb, D.; Rechkemmer, G.; Briviba, K. Malvidin-3-glucoside bioavailability in humans after ingestion of red wine, dealcoholized red wine and red grape juice. Eur. J. Nutr. 2001, 40, 113–120. [CrossRef] 104. Balentine, D.A.; Wiseman, S.A.; Bouwens, L.C.M. The chemistry of tea flavonoids. Crit. Rev. Food Sci. Nutr. 1997, 37, 693–704. [CrossRef][PubMed] 105. Hollman, P.C.H.; Hof, K.H.V.H.; Tijburg, L.B.M.; Katan, M.B. Addition of milk does not affect the absorption of flavonols from tea in man. Free Radic. Res. 2001, 34, 297–300. [CrossRef] 106. Rafiq, S.; Kaul, R.; Sofi, S.A.; Bashir, N.; Nazir, F.; Ahmad Nayik, G. Citrus peel as a source of functional ingredient: A review. J. Saudi Soc. Agric. Sci. 2018, 17, 351–358. [CrossRef] Molecules 2021, 26, 2959 34 of 35

107. Pérez-Jiménez, J.; Saura-Calixto, F. Fruit peels as sources of non-extractable polyphenols or macromolecular antioxidants: Analysis and nutritional implications. Food Res. Int. 2018, 111, 148–152. [CrossRef][PubMed] 108. Ewald, C.; Fjelkner-Modig, S.; Johansson, K.; Sjöholm, I.; Åkesson, B. Effect of processing on major flavonoids in processed onions, green beans, and peas. Food Chem. 1999, 64, 231–235. [CrossRef] 109. Kwak, J.H.; Seo, J.M.; Kim, N.H.; Arasu, M.V.; Kim, S.; Yoon, M.K.; Kim, S.J. Variation of quercetin glycoside derivatives in three onion (Allium cepa L.) varieties. Saudi J. Biol. Sci. 2017, 24, 1387–1391. [CrossRef] 110. Talcott, S.T.; Howard, L.R.; Brenes, C.H. Contribution of peridern material and blanching time to the quality of pasteurized peach puree. J. Agric. Food Chem. 2000, 48, 4590–4596. [CrossRef] 111. Asami, D.K.; Hong, Y.-J.; Barrett, D.M.; Mitchell, A.E. Processing-induced changes in total phenolics and procyanidins in clingstone peaches. J. Sci. Food Agric. 2003, 83, 56–63. [CrossRef] 112. Lamçe, F.; Gozhdari, K.; Kongoli, R.; Meta, B.; Kyçyk, O. Evaluation of the content of polyphenols and flavonoids during the fermentation of white wines (cv. Pulëz and Shesh i bardhë) with and without skins. Albanian J. Agric. Sci. 2018, 568–571. 113. Murthy, C.T.; Rani, M.; Rao, P.N.S. Optimal grinding characteristics of black pepper for essential oil yield. J. Food Process. Eng. 1999, 22, 161–173. [CrossRef] 114. Becker, L.; Zaiter, A.; Petit, J.; Karam, M.-C.; Sudol, M.; Baudelaire, E.; Scher, J.; Dicko, A. How do grinding and sieving impact on physicochemical properties, polyphenol content, and antioxidant activity of Hieracium pilosella L. powders? J. Funct. Foods 2017, 35, 666–672. [CrossRef] 115. Derossi, A.; Ricci, I.; Caporizzi, R.; Fiore, A.; Severini, C. How grinding level and brewing method (Espresso, American, Turkish) could affect the antioxidant activity and bioactive compounds in a coffee cup. J. Sci. Food Agric. 2018, 98, 3198–3207. [CrossRef] 116. Hu, J.; Chen, Y.; Ni, D. Effect of superfine grinding on quality and antioxidant property of fine green tea powders. LWT Food Sci. Technol. 2012, 45, 8–12. [CrossRef] 117. Augusto-Obara, T.R.; de Oliveira, J.; da Gloria, E.M.; Spoto, M.H.F.; Godoy, K.; de Souza Vieira, T.M.F.; Scheuermann, E. Benefits of superfine grinding method on antioxidant and antifungal characteristic of Brazilian green propolis extract. Sci. Agric. 2019, 76, 398–404. [CrossRef]

118. Calugar, P.C.; Coldea, T.E.; Salant, ă, L.C.; Pop, C.R.; Pasqualone, A.; Burja-Udrea, C.; Zhao, H.; Mudura, E. An Overview of the Factors Influencing Apple Cider Sensory and Microbial Quality from Raw Materials to Emerging Processing Technologies. Processes 2021, 9, 502. [CrossRef] 119. Li, S.; Zhang, R.; Lei, D.; Huang, Y.; Cheng, S.; Zhu, Z.; Wu, Z.; Cravotto, G. Impact of ultrasound, microwaves and high-pressure processing on food components and their interactions. Trends Food Sci. Technol. 2021, 109, 1–15. [CrossRef] 120. Klepacka, J.; Najda, A. Effect of commercial processing on polyphenols and antioxidant activity of seeds. Int. J. Food Sci. Technol. 2021, 56, 661–670. [CrossRef] 121. Wani, S.M.; Masoodi, F.; Haq, E.; Ahmad, M.; Ganai, S. Influence of processing methods and storage on phenolic compounds and carotenoids of apricots. LWT 2020, 132, 109846. [CrossRef] 122. Wani, S.M.; Masoodi, F.; Yousuf, S.; Dar, B.; Rather, S. Phenolic compounds and antiproliferative activity of apricots: Influence of canning, freezing, and drying. J. Food Process. Preserv. 2020, 44, e14887. [CrossRef] 123. Orphanides, A.; Goulas, V.; Gekas, V. Effect of Drying Method on the Phenolic Content and Antioxidant Capacity of Spearmint. Czech. J. Food Sci 2013, 31, 509–513. [CrossRef] 124. Alfaro, S.; Mutis, A.; Quiroz, A.; Seguel, I.; Scheuermann, E. Effects of Drying Techniques on Murtilla Fruit Polyphenols and Antioxidant Activity. J. Food Res. 2014, 3, 73. [CrossRef] 125. Yuste, S.; Macià, A.; Motilva, M.-J.; Prieto-Diez, N.; Romero, M.-P.; Pedret, A.; Solà, R.; Ludwig, I.A.; Rubió, L. Thermal and non-thermal processing of red-fleshed apple: How are (poly) phenol composition and bioavailability affected? Food Funct. 2020, 11, 10436–10447. [CrossRef] 126. Arfaoui, L. Total polyphenol content and radical scavenging activity of functional yogurt enriched with dates. Czech. J. Food Sci. 2020, 38, 287–292. [CrossRef] 127. Fang, Z.; Hu, Y.; Liu, D.; Chen, J.; Ye, X. Changes of phenolic acids and antioxidant activities during potherb mustard (Brassica juncea, Coss.) pickling. Food Chem. 2008, 108, 811–817. [CrossRef][PubMed] 128. Nurul, S.; Asmah, R. Evaluation of antioxidant properties in fresh and pickled papaya. Int. Food Res. J. 2012, 19, 1117. 129. Sayin, K.F.; Alkan, S.B. The effect of pickling on total phenolic contents and antioxidant activity of 10 vegetables. J. Food Health Sci. 2015, 1, 135–141. [CrossRef] 130. Chung, I.-M.; Oh, J.-Y.; Kim, S.-H. Comparative study of phenolic compounds, vitamin E, and fatty acids compositional profiles in black seed-coated soybeans (Glycine Max (L.) Merrill) depending on pickling period in brewed vinegar. Chem. Cent. J. 2017, 11, 64. [CrossRef] 131. Rodríguez-Roque, M.J.; de Ancos, B.; Sánchez-Moreno, C.; Cano, M.P.; Elez-Martínez, P.; Martín-Belloso, O. Impact of food matrix and processing on the in vitro bioaccessibility of vitamin C, phenolic compounds, and hydrophilic antioxidant activity from fruit juice-based beverages. J. Funct. Foods 2015, 14, 33–43. [CrossRef] 132. He, Z.; Tao, Y.; Zeng, M.; Zhang, S.; Tao, G.; Qin, F.; Chen, J. High pressure homogenization processing, thermal treatment and milk matrix affect in vitro bioaccessibility of phenolics in apple, grape and orange juice to different extents. Food Chem. 2016, 200, 107–116. [CrossRef] Molecules 2021, 26, 2959 35 of 35

133. Kamiloglu, S. Effect of different freezing methods on the bioaccessibility of strawberry polyphenols. Int. J. Food Sci. Technol. 2019, 54, 2652–2660. [CrossRef] 134. Castello, F.; Fernández-Pachón, M.-S.; Cerrillo, I.; Escudero-López, B.; Ortega, Á.; Rosi, A.; Bresciani, L.; Del Rio, D.; Mena, P. Absorption, metabolism, and excretion of orange juice (poly) phenols in humans: The effect of a controlled alcoholic fermentation. Arch. Biochem. Biophys. 2020, 695, 108627. [CrossRef]